Dépouillements

Stress and handicap / Martin C. O. BAX in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.285-286 Titre : Stress and handicap Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1980 Article en page(s) : p.285-286 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=508 [article] Stress and handicap [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1980 . - p.285-286. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.285-286 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=508

Surgical correction of equinus deformity in cerebral palsy / Christopher LEE in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.287-92 Titre : Surgical correction of equinus deformity in cerebral palsy Type de document : Texte imprimé et/ou numérique Auteurs : Christopher LEE, Auteur ; Eugene E. BLECK, Auteur Année de publication : 1980 Article en page(s) : p.287-92 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Sixty-seven children who had been operated on for equinus deformity due to spastic cerebral palsy were studied retrospectively. The recurrence rate of equinus after 51 Baker-Strayer gastrocnemius lengthenings was 29 per cent, and aftef the sliding Hoke type of tendo calcaneus lengthenings it was 9 per cent. In both groups the postoperative care was the same: no bracing, no night splints, and no stretching. The recurrence rate of equinus after tendo calcaneus lengthening is comparable with other reported series. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=508 [article] Surgical correction of equinus deformity in cerebral palsy [Texte imprimé et/ou numérique] / Christopher LEE, Auteur ; Eugene E. BLECK, Auteur . - 1980 . - p.287-92. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.287-92 Index. décimale : PER Périodiques Résumé : Sixty-seven children who had been operated on for equinus deformity due to spastic cerebral palsy were studied retrospectively. The recurrence rate of equinus after 51 Baker-Strayer gastrocnemius lengthenings was 29 per cent, and aftef the sliding Hoke type of tendo calcaneus lengthenings it was 9 per cent. In both groups the postoperative care was the same: no bracing, no night splints, and no stretching. The recurrence rate of equinus after tendo calcaneus lengthening is comparable with other reported series. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=508

A non-surgical method of reducing drooling in cerebral-palsied children / Margaret M. HARRIS in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.293-299 Titre : A non-surgical method of reducing drooling in cerebral-palsied children Type de document : Texte imprimé et/ou numérique Auteurs : Margaret M. HARRIS, Auteur ; Peter F. DIGNAM, Auteur Année de publication : 1980 Article en page(s) : p.293-299 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A programme is described which aimed to reduce drooling volume in groups of cerebral-palsied children. The programme, which lasted one year, required the children to wear chin cups and to attend special 'anti-drooling' classes. The over-all reduction in volume of drooling was 73 per cent. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=508 [article] A non-surgical method of reducing drooling in cerebral-palsied children [Texte imprimé et/ou numérique] / Margaret M. HARRIS, Auteur ; Peter F. DIGNAM, Auteur . - 1980 . - p.293-299. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.293-299 Index. décimale : PER Périodiques Résumé : A programme is described which aimed to reduce drooling volume in groups of cerebral-palsied children. The programme, which lasted one year, required the children to wear chin cups and to attend special 'anti-drooling' classes. The over-all reduction in volume of drooling was 73 per cent. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=508

Cerebrospinal fluid lactate dehydrogenase in infants with perinatal asphyxia / Robert T. HALL in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.300-307 Titre : Cerebrospinal fluid lactate dehydrogenase in infants with perinatal asphyxia Type de document : Texte imprimé et/ou numérique Auteurs : Robert T. HALL, Auteur ; Prakash B. KULKARNI, Auteur ; Michael B. SHEEHAN, Auteur ; Philip G. RHODES, Auteur Année de publication : 1980 Article en page(s) : p.300-307 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Cerebrospinal fluid (CSF) lactate dehydrogenase was determined in 19 control infants without asphyxia (Group I), 24 infants with perinatal asphyxia (Group II), and 26 asphyxiated infants with seizures (Group III). Mean birthweights, gestational ages, CSF glucose, protein and red blood cells, and the ages at which the lumbar punctures were performed were not significantly different among the three groups. Mean CSF lactate dehydrogenase was significantly higher in Group III than in Groups I and II. Isoenzyme patterns indicated that the origin of the CSF lactate dehydrogenase was neuronal tissue, or a plasma transudate from increased permeability of the blood-brain barrier. There were 10 deaths due to anoxic encephalopathy in Group III, but none in Groups I or II. Follow-up of survivors at 10 to 30 months of age revealed neurological sequelae in three infants in Group I, two in Group II and five in Group III. Mean CSF lactate dehydrogenase in those with sequelae had not been significantly different from that of normal survivors; however, the mean was significantly higher in infants who died with anoxic encephalopathy compared with normal infants. These data indicate that CSF lactate dehydrogenase is significantly elevated in infants with fatal anoxic brain damage, and suggest that determinations may be of prognostic value in non-fatal cerebral hypoxia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Cerebrospinal fluid lactate dehydrogenase in infants with perinatal asphyxia [Texte imprimé et/ou numérique] / Robert T. HALL, Auteur ; Prakash B. KULKARNI, Auteur ; Michael B. SHEEHAN, Auteur ; Philip G. RHODES, Auteur . - 1980 . - p.300-307. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.300-307 Index. décimale : PER Périodiques Résumé : Cerebrospinal fluid (CSF) lactate dehydrogenase was determined in 19 control infants without asphyxia (Group I), 24 infants with perinatal asphyxia (Group II), and 26 asphyxiated infants with seizures (Group III). Mean birthweights, gestational ages, CSF glucose, protein and red blood cells, and the ages at which the lumbar punctures were performed were not significantly different among the three groups. Mean CSF lactate dehydrogenase was significantly higher in Group III than in Groups I and II. Isoenzyme patterns indicated that the origin of the CSF lactate dehydrogenase was neuronal tissue, or a plasma transudate from increased permeability of the blood-brain barrier. There were 10 deaths due to anoxic encephalopathy in Group III, but none in Groups I or II. Follow-up of survivors at 10 to 30 months of age revealed neurological sequelae in three infants in Group I, two in Group II and five in Group III. Mean CSF lactate dehydrogenase in those with sequelae had not been significantly different from that of normal survivors; however, the mean was significantly higher in infants who died with anoxic encephalopathy compared with normal infants. These data indicate that CSF lactate dehydrogenase is significantly elevated in infants with fatal anoxic brain damage, and suggest that determinations may be of prognostic value in non-fatal cerebral hypoxia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Cerebral oxidative metabolism in perinatal post-hemorrhagic hydrocephalus / Robert C. VANNUCCI in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.308-316 Titre : Cerebral oxidative metabolism in perinatal post-hemorrhagic hydrocephalus Type de document : Texte imprimé et/ou numérique Auteurs : Robert C. VANNUCCI, Auteur ; Jonathan HELLMAN, Auteur ; Orest DUBYNSKY, Auteur Année de publication : 1980 Article en page(s) : p.308-316 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Survivors of perinatal intraventricular hemorrhage often develop a distinct clinical syndrome characterized by hydrocephalus and biochemical abnormalities in cerebrospinal fluid. The authors investigated six neonates with post-hemorrhagic obstructive hydrocephalus in order to identify cerebral metabolic disturbances responsible for the hypoglycorrhachia observed in this disorder. Lactic acid concentraions and lactate/pyruvate ratios in ventricular fluid were significantly elevated in infants with post-hemorrhagic hydrocephalus compared with the values in five with congenital (non-hemorrhagic) obstructive hydrocephalus. Comparable degrees of ventricular dilatation and intracranial hypertension were present in the two groups. There is evidence that neither residual cellular elements in ventricular fluid nor a disrupted blood-CSF barrier can fully explain the observed alterations in ventricular-fluid glucose, lactate or lactate/pyruvate ratios. It is suggested that when periventricular hemorrhage occurs, the associated cerebral ischemia leads to focal anaerobic glycolysis and increased glucose requirement. With inadequate cerebral glucose glycolysis and increased glucose requirement. With inadequate cerebral glucose delivery from the blood, glucose diffuses into the brain from the ventricular fluid, resulting in hypoglycorrhachia. Cerebral lactic acid production is enhanced, which accumulates in ventricular fluid in the presence of ventricular obstruction. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Cerebral oxidative metabolism in perinatal post-hemorrhagic hydrocephalus [Texte imprimé et/ou numérique] / Robert C. VANNUCCI, Auteur ; Jonathan HELLMAN, Auteur ; Orest DUBYNSKY, Auteur . - 1980 . - p.308-316. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.308-316 Index. décimale : PER Périodiques Résumé : Survivors of perinatal intraventricular hemorrhage often develop a distinct clinical syndrome characterized by hydrocephalus and biochemical abnormalities in cerebrospinal fluid. The authors investigated six neonates with post-hemorrhagic obstructive hydrocephalus in order to identify cerebral metabolic disturbances responsible for the hypoglycorrhachia observed in this disorder. Lactic acid concentraions and lactate/pyruvate ratios in ventricular fluid were significantly elevated in infants with post-hemorrhagic hydrocephalus compared with the values in five with congenital (non-hemorrhagic) obstructive hydrocephalus. Comparable degrees of ventricular dilatation and intracranial hypertension were present in the two groups. There is evidence that neither residual cellular elements in ventricular fluid nor a disrupted blood-CSF barrier can fully explain the observed alterations in ventricular-fluid glucose, lactate or lactate/pyruvate ratios. It is suggested that when periventricular hemorrhage occurs, the associated cerebral ischemia leads to focal anaerobic glycolysis and increased glucose requirement. With inadequate cerebral glucose glycolysis and increased glucose requirement. With inadequate cerebral glucose delivery from the blood, glucose diffuses into the brain from the ventricular fluid, resulting in hypoglycorrhachia. Cerebral lactic acid production is enhanced, which accumulates in ventricular fluid in the presence of ventricular obstruction. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

The behavior of jaundiced infants undergoing phototherapy / R. W. TELZROW in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.317-326 Titre : The behavior of jaundiced infants undergoing phototherapy Type de document : Texte imprimé et/ou numérique Auteurs : R. W. TELZROW, Auteur ; Thomas Berry BRAZELTON, Auteur ; Edward Z. TRONICK, Auteur ; D. M. SNYDER, Auteur Année de publication : 1980 Article en page(s) : p.317-326 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Ten full-term jaundiced infants were examined with the Brazelton Scale before, during and following phototherapy. They were compared with 10 non-jaundiced control infants examined at the same post-partum ages. All infants were appropriate for gestational age and free of perinatal complications other than hyperbilirubinemia. Differences on the orienting items of the Brazelton examinations (primarily visual orienting) were found prior to the onset of phototherapy or separation, and persisted for the length of the study. The greatest over-all differences were noted during phototherapy and separation from the mother, at which times the treatment group had lower scores on four of the six orienting items. They also had lower scores on muscle tonus, pull-to-sit and cuddliness while undergoing phototherapy, and poorer scores on orienting items, self-quieting and tremulousness were also evident three days following treatment. It is suggested that the differences found in mother-infant interaction following separation for the management of minor medical problems may be related to changes in infant behaviour which are already evident prior to separation. In the cases of jaundiced infants requiring phototherapy, these changes appear to be related primarily to hyperbilirubinemia. The possibility of these effects being prolonged or confounded by phototherapy or separation cannot be discounted. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] The behavior of jaundiced infants undergoing phototherapy [Texte imprimé et/ou numérique] / R. W. TELZROW, Auteur ; Thomas Berry BRAZELTON, Auteur ; Edward Z. TRONICK, Auteur ; D. M. SNYDER, Auteur . - 1980 . - p.317-326. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.317-326 Index. décimale : PER Périodiques Résumé : Ten full-term jaundiced infants were examined with the Brazelton Scale before, during and following phototherapy. They were compared with 10 non-jaundiced control infants examined at the same post-partum ages. All infants were appropriate for gestational age and free of perinatal complications other than hyperbilirubinemia. Differences on the orienting items of the Brazelton examinations (primarily visual orienting) were found prior to the onset of phototherapy or separation, and persisted for the length of the study. The greatest over-all differences were noted during phototherapy and separation from the mother, at which times the treatment group had lower scores on four of the six orienting items. They also had lower scores on muscle tonus, pull-to-sit and cuddliness while undergoing phototherapy, and poorer scores on orienting items, self-quieting and tremulousness were also evident three days following treatment. It is suggested that the differences found in mother-infant interaction following separation for the management of minor medical problems may be related to changes in infant behaviour which are already evident prior to separation. In the cases of jaundiced infants requiring phototherapy, these changes appear to be related primarily to hyperbilirubinemia. The possibility of these effects being prolonged or confounded by phototherapy or separation cannot be discounted. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Dissociated visual development: electrodiagnostic studies in infants who are 'slow to see' / David H. MELLOR in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.327-335 Titre : Dissociated visual development: electrodiagnostic studies in infants who are 'slow to see' Type de document : Texte imprimé et/ou numérique Auteurs : David H. MELLOR, Auteur ; Alistair R. FIELDER, Auteur Année de publication : 1980 Article en page(s) : p.327-335 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Four infants were studied who failed to show any visual interest or following responses in the first three months of life. Although no definite ocular abnormalities were found at the time of presentation, both the parents and their medical advisers initially had serious concerns about the infants' visual prognosis. Initial electroretinograms (ERG) were found to be unequivocally normal, but three of the infants showed absent or impaired cortical visual evoked responses (VER). The fourth infant had an initial VER which was immature. Subsequently, all the infants showed increasing visual responsiveness from three to four months of age and all now have visual behaviour and general development appropriate to their ages. The VERs were repeated after four months of age and all showed normal responses. It is concluded that poor or even absent VER responses in early infancy may not always indicate a poor prognosis for vision. The possible mechanisms of this visual maturational lag are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Dissociated visual development: electrodiagnostic studies in infants who are 'slow to see' [Texte imprimé et/ou numérique] / David H. MELLOR, Auteur ; Alistair R. FIELDER, Auteur . - 1980 . - p.327-335. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.327-335 Index. décimale : PER Périodiques Résumé : Four infants were studied who failed to show any visual interest or following responses in the first three months of life. Although no definite ocular abnormalities were found at the time of presentation, both the parents and their medical advisers initially had serious concerns about the infants' visual prognosis. Initial electroretinograms (ERG) were found to be unequivocally normal, but three of the infants showed absent or impaired cortical visual evoked responses (VER). The fourth infant had an initial VER which was immature. Subsequently, all the infants showed increasing visual responsiveness from three to four months of age and all now have visual behaviour and general development appropriate to their ages. The VERs were repeated after four months of age and all showed normal responses. It is concluded that poor or even absent VER responses in early infancy may not always indicate a poor prognosis for vision. The possible mechanisms of this visual maturational lag are discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Infant neurological abnormalities as indicators of cognitive impairment / Rosalyn A. RUBIN in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.336-343 Titre : Infant neurological abnormalities as indicators of cognitive impairment Type de document : Texte imprimé et/ou numérique Auteurs : Rosalyn A. RUBIN, Auteur ; Bruce BALOW, Auteur Année de publication : 1980 Article en page(s) : p.336-343 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : In a prospective longitudinal study, 1319 children who had received three neurological examinations during their first year of life were administered measures of cognitive development and academic achievement up to and including 12 years of age. With both social class and birthweight statistically controlled, children identified as neurologically suspect or abnormal on more than one of the infant examinations (N = 22) consistently performed far below control children on measures of intelligence, motor skills, language development and school achievement. Children who had been neurologically suspect or abnormal on only one infant examination (N = 165) performed significantly less well than those never suspected of neurological abnormality in infancy (N = 1132). Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Infant neurological abnormalities as indicators of cognitive impairment [Texte imprimé et/ou numérique] / Rosalyn A. RUBIN, Auteur ; Bruce BALOW, Auteur . - 1980 . - p.336-343. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.336-343 Index. décimale : PER Périodiques Résumé : In a prospective longitudinal study, 1319 children who had received three neurological examinations during their first year of life were administered measures of cognitive development and academic achievement up to and including 12 years of age. With both social class and birthweight statistically controlled, children identified as neurologically suspect or abnormal on more than one of the infant examinations (N = 22) consistently performed far below control children on measures of intelligence, motor skills, language development and school achievement. Children who had been neurologically suspect or abnormal on only one infant examination (N = 165) performed significantly less well than those never suspected of neurological abnormality in infancy (N = 1132). Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Factors affecting sleep spindle activity during infancy / Hen-Shin WU in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.344-351 Titre : Factors affecting sleep spindle activity during infancy Type de document : Texte imprimé et/ou numérique Auteurs : Hen-Shin WU, Auteur ; Austin LEE, Auteur ; Jeffrey GOULD, Auteur ; Naomi FINEBERG, Auteur Année de publication : 1980 Article en page(s) : p.344-351 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Sleep spindle activity was evaluated in 32 twins at 52 weeks postconceptional age. Significantly increased mature spindle activity was seen in infants born at older gestational ages, in femals, and in infants who were stressed by intra-uterine growth retardation or with mild postnatal respiratory illness. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Factors affecting sleep spindle activity during infancy [Texte imprimé et/ou numérique] / Hen-Shin WU, Auteur ; Austin LEE, Auteur ; Jeffrey GOULD, Auteur ; Naomi FINEBERG, Auteur . - 1980 . - p.344-351. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.344-351 Index. décimale : PER Périodiques Résumé : Sleep spindle activity was evaluated in 32 twins at 52 weeks postconceptional age. Significantly increased mature spindle activity was seen in infants born at older gestational ages, in femals, and in infants who were stressed by intra-uterine growth retardation or with mild postnatal respiratory illness. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Deficits in space-form perception in patients with sex chromosome mosaicism (45,X/46,XY) / Allan J. EBBIN in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.352-361 Titre : Deficits in space-form perception in patients with sex chromosome mosaicism (45,X/46,XY) Type de document : Texte imprimé et/ou numérique Auteurs : Allan J. EBBIN, Auteur ; Valeta V. HOWELL, Auteur ; Miriam G. WILSON, Auteur Année de publication : 1980 Article en page(s) : p.352-361 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Several studies have shown that selective deficits in space-form perception are found in patients with Turner's syndrome, associated with 45,X or a structural anomaly of an X chromosome. The authors sought to determine whether significant deviations from normal or from Turner's syndrome (relative to space perception) occur when a Y chromosome is present. The four patients studied, aged between 4 1/2 and 24 years, had a karyotype of 45,X/46,XY and a phenotype ranging from sexual ambiguity at birth to typical Turner's syndrome. Although all were in the normal intelligence range (IQ 80 or above), on testing they demonstrated below-average ability in tasks involving visualization of spatial forms, and their drawings were generally immature. The results suggest that patients with sex chromosome mosaicism X/XY may have similar deficits in space-form perception and orientation to those previously demonstrated in Turner's syndrome. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Deficits in space-form perception in patients with sex chromosome mosaicism (45,X/46,XY) [Texte imprimé et/ou numérique] / Allan J. EBBIN, Auteur ; Valeta V. HOWELL, Auteur ; Miriam G. WILSON, Auteur . - 1980 . - p.352-361. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.352-361 Index. décimale : PER Périodiques Résumé : Several studies have shown that selective deficits in space-form perception are found in patients with Turner's syndrome, associated with 45,X or a structural anomaly of an X chromosome. The authors sought to determine whether significant deviations from normal or from Turner's syndrome (relative to space perception) occur when a Y chromosome is present. The four patients studied, aged between 4 1/2 and 24 years, had a karyotype of 45,X/46,XY and a phenotype ranging from sexual ambiguity at birth to typical Turner's syndrome. Although all were in the normal intelligence range (IQ 80 or above), on testing they demonstrated below-average ability in tasks involving visualization of spatial forms, and their drawings were generally immature. The results suggest that patients with sex chromosome mosaicism X/XY may have similar deficits in space-form perception and orientation to those previously demonstrated in Turner's syndrome. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Joubert syndrome: a case confirmed by computerized tomography / Paolo CURATOLO in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.362-6 Titre : Joubert syndrome: a case confirmed by computerized tomography Type de document : Texte imprimé et/ou numérique Auteurs : Paolo CURATOLO, Auteur ; Sandro MERCURI, Auteur ; Enrico COTRONEO, Auteur Année de publication : 1980 Article en page(s) : p.362-6 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The authors report a new case of Joubert syndrome (agenesis of the cerebellar vermis, mental retardation, disturbance of respiratory rhythm, ataxia, abnormal eye-movements) and review the relevant literature on the other nine cases reported. The diagnosis in the present case was confirmed by computerized tomography. Early recognition of this syndrome is important in view of the prognosis and for genetic counseling. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Joubert syndrome: a case confirmed by computerized tomography [Texte imprimé et/ou numérique] / Paolo CURATOLO, Auteur ; Sandro MERCURI, Auteur ; Enrico COTRONEO, Auteur . - 1980 . - p.362-6. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.362-6 Index. décimale : PER Périodiques Résumé : The authors report a new case of Joubert syndrome (agenesis of the cerebellar vermis, mental retardation, disturbance of respiratory rhythm, ataxia, abnormal eye-movements) and review the relevant literature on the other nine cases reported. The diagnosis in the present case was confirmed by computerized tomography. Early recognition of this syndrome is important in view of the prognosis and for genetic counseling. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Accidental glibenclamide ingestion in an infant: clinical and electroencephalographic aspects / Lorenzo PAVONE in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.366-371 Titre : Accidental glibenclamide ingestion in an infant: clinical and electroencephalographic aspects Type de document : Texte imprimé et/ou numérique Auteurs : Lorenzo PAVONE, Auteur ; Florindo MOLLICA, Auteur ; S. MUSUMECI, Auteur ; S. MARINO, Auteur ; G. PAMPIGLIONE, Auteur Année de publication : 1980 Article en page(s) : p.366-371 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The clinical and EEG features of an infant during and after a severe episode of glibenclamide-induced hypoglycaemia are reported, with a 12-month follow-up. The very few cases reported in the literature, together with the present report, suggest that the neurological sequelae of severe hypoglycaemia resulting from ingestion of this drug are due to more patchy involvement of the central nervous system than would be expected from experimental work on hypoglycaemia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Accidental glibenclamide ingestion in an infant: clinical and electroencephalographic aspects [Texte imprimé et/ou numérique] / Lorenzo PAVONE, Auteur ; Florindo MOLLICA, Auteur ; S. MUSUMECI, Auteur ; S. MARINO, Auteur ; G. PAMPIGLIONE, Auteur . - 1980 . - p.366-371. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.366-371 Index. décimale : PER Périodiques Résumé : The clinical and EEG features of an infant during and after a severe episode of glibenclamide-induced hypoglycaemia are reported, with a 12-month follow-up. The very few cases reported in the literature, together with the present report, suggest that the neurological sequelae of severe hypoglycaemia resulting from ingestion of this drug are due to more patchy involvement of the central nervous system than would be expected from experimental work on hypoglycaemia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Arthrogryposis multiplex congenita due to congenital myasthenia / L. M. E. SMIT in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.371-374 Titre : Arthrogryposis multiplex congenita due to congenital myasthenia Type de document : Texte imprimé et/ou numérique Auteurs : L. M. E. SMIT, Auteur ; P. G. BARTH, Auteur Année de publication : 1980 Article en page(s) : p.371-374 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Decreased fetal movements may cause arthrogryposis multiplex congenita. Several distinct neuromuscular disorders may cause this syndrome, but congenital myasthenia has not previously been considered to be a possible cause. The authors report a case of congenital myasthenia gravis leading to arthrogryposis congenita. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509 [article] Arthrogryposis multiplex congenita due to congenital myasthenia [Texte imprimé et/ou numérique] / L. M. E. SMIT, Auteur ; P. G. BARTH, Auteur . - 1980 . - p.371-374. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.371-374 Index. décimale : PER Périodiques Résumé : Decreased fetal movements may cause arthrogryposis multiplex congenita. Several distinct neuromuscular disorders may cause this syndrome, but congenital myasthenia has not previously been considered to be a possible cause. The authors report a case of congenital myasthenia gravis leading to arthrogryposis congenita. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=509

Computer-assisted cranial tomography in tuberous sclerosis / Norman C. NEVIN in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.379-380 Titre : Computer-assisted cranial tomography in tuberous sclerosis Type de document : Texte imprimé et/ou numérique Auteurs : Norman C. NEVIN, Auteur Année de publication : 1980 Article en page(s) : p.379-380 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Computer-assisted cranial tomography in tuberous sclerosis [Texte imprimé et/ou numérique] / Norman C. NEVIN, Auteur . - 1980 . - p.379-380. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.379-380 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Reflex anoxic seizures and ocular compression / J. B. STEPHENSON in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.380-386 Titre : Reflex anoxic seizures and ocular compression Type de document : Texte imprimé et/ou numérique Auteurs : J. B. STEPHENSON, Auteur Année de publication : 1980 Article en page(s) : p.380-386 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Reflex anoxic seizures and ocular compression [Texte imprimé et/ou numérique] / J. B. STEPHENSON, Auteur . - 1980 . - p.380-386. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.380-386 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Peroneal muscular atrophy in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.386-390 Titre : Peroneal muscular atrophy Type de document : Texte imprimé et/ou numérique Année de publication : 1980 Article en page(s) : p.386-390 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Peroneal muscular atrophy [Texte imprimé et/ou numérique] . - 1980 . - p.386-390. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.386-390 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Life stress, illness and social supports / Robert J. HAGGERTY in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.391-400 Titre : Life stress, illness and social supports Type de document : Texte imprimé et/ou numérique Auteurs : Robert J. HAGGERTY, Auteur Année de publication : 1980 Article en page(s) : p.391-400 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Stress has been shown to lower resistance to disease and thus to have a significant effect on susceptibility to a variety of physical and psychological illnesses. A correlation has also been established between the degree of social stress and an individual's use of medical services. However, the majority of people do not respond to stress in these ways. Social supports (e.g. a caring family) seem to be an important protective factor against the effects of stress. Other mtethods of protection (meditation, relaxation response or learning specific coping skills) are also important, but have been little studied. Given their importance in preventive medicine, the author suggests that social support systems should pay an increasing part in health services. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Life stress, illness and social supports [Texte imprimé et/ou numérique] / Robert J. HAGGERTY, Auteur . - 1980 . - p.391-400. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.391-400 Index. décimale : PER Périodiques Résumé : Stress has been shown to lower resistance to disease and thus to have a significant effect on susceptibility to a variety of physical and psychological illnesses. A correlation has also been established between the degree of social stress and an individual's use of medical services. However, the majority of people do not respond to stress in these ways. Social supports (e.g. a caring family) seem to be an important protective factor against the effects of stress. Other mtethods of protection (meditation, relaxation response or learning specific coping skills) are also important, but have been little studied. Given their importance in preventive medicine, the author suggests that social support systems should pay an increasing part in health services. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Controversies about Duchenne muscular dystrophy / Ernest W. JOHNSON in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.401-402 Titre : Controversies about Duchenne muscular dystrophy Type de document : Texte imprimé et/ou numérique Auteurs : Ernest W. JOHNSON, Auteur Année de publication : 1980 Article en page(s) : p.401-402 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Controversies about Duchenne muscular dystrophy [Texte imprimé et/ou numérique] / Ernest W. JOHNSON, Auteur . - 1980 . - p.401-402. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.401-402 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Neurological complications of cystinuria / Jennifer DAVIS in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.402-403 Titre : Neurological complications of cystinuria Type de document : Texte imprimé et/ou numérique Auteurs : Jennifer DAVIS, Auteur ; David C. TAYLOR, Auteur Année de publication : 1980 Article en page(s) : p.402-403 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Neurological complications of cystinuria [Texte imprimé et/ou numérique] / Jennifer DAVIS, Auteur ; David C. TAYLOR, Auteur . - 1980 . - p.402-403. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.402-403 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Neurological explanation / Paul R. MILLER in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.404 Titre : Neurological explanation Type de document : Texte imprimé et/ou numérique Auteurs : Paul R. MILLER, Auteur Année de publication : 1980 Article en page(s) : p.404 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Neurological explanation [Texte imprimé et/ou numérique] / Paul R. MILLER, Auteur . - 1980 . - p.404. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.404 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Hypersensitivity to auditory stimulation during administration of the Neonatal Neurobehavioral Assessment Scale / Marilyn L. RIESE in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.404-405 Titre : Hypersensitivity to auditory stimulation during administration of the Neonatal Neurobehavioral Assessment Scale Type de document : Texte imprimé et/ou numérique Auteurs : Marilyn L. RIESE, Auteur Année de publication : 1980 Article en page(s) : p.404-405 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Hypersensitivity to auditory stimulation during administration of the Neonatal Neurobehavioral Assessment Scale [Texte imprimé et/ou numérique] / Marilyn L. RIESE, Auteur . - 1980 . - p.404-405. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.404-405 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Behavioural treatment of Lesch-Nyhan syndrome / Francesca LA VECCHIO in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.405-407 Titre : Behavioural treatment of Lesch-Nyhan syndrome Type de document : Texte imprimé et/ou numérique Auteurs : Francesca LA VECCHIO, Auteur Année de publication : 1980 Article en page(s) : p.405-407 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Behavioural treatment of Lesch-Nyhan syndrome [Texte imprimé et/ou numérique] / Francesca LA VECCHIO, Auteur . - 1980 . - p.405-407. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.405-407 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Developmental dyspraxia and verbal dyspraxia / Ivan LESNY in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.407 Titre : Developmental dyspraxia and verbal dyspraxia Type de document : Texte imprimé et/ou numérique Auteurs : Ivan LESNY, Auteur Année de publication : 1980 Article en page(s) : p.407 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510 [article] Developmental dyspraxia and verbal dyspraxia [Texte imprimé et/ou numérique] / Ivan LESNY, Auteur . - 1980 . - p.407. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.407 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=510

Sandifer syndrome: an unappreciated clinical entity / Steven L. WERLIN in Developmental Medicine & Child Neurology, 22-3 (June 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-3 (June 1980) . - p.374-378 Titre : Sandifer syndrome: an unappreciated clinical entity Type de document : Texte imprimé et/ou numérique Auteurs : Steven L. WERLIN, Auteur ; Bernard J. D'SOUZA, Auteur ; Walter J. HOGAN, Auteur ; Wylie J. DODDS, Auteur ; Ronald C. ARNDOFER, Auteur Année de publication : 1980 Article en page(s) : p.374-378 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Five cases of Sandifer syndrome are reported, and the authors suggest that frequently the diagnosis may be overlooked, especially when the patient has a milder or incomplete form of the syndrome. None of the children had hiatal hernia, so this is not an essential requirement for the syndrome. The findings in these five cases suggest that the abnormal posturing associated with this syndrome may be the result of extreme sensitivity of the esophagus to refluxed gastric acid. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=511 [article] Sandifer syndrome: an unappreciated clinical entity [Texte imprimé et/ou numérique] / Steven L. WERLIN, Auteur ; Bernard J. D'SOUZA, Auteur ; Walter J. HOGAN, Auteur ; Wylie J. DODDS, Auteur ; Ronald C. ARNDOFER, Auteur . - 1980 . - p.374-378. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-3 (June 1980) . - p.374-378 Index. décimale : PER Périodiques Résumé : Five cases of Sandifer syndrome are reported, and the authors suggest that frequently the diagnosis may be overlooked, especially when the patient has a milder or incomplete form of the syndrome. None of the children had hiatal hernia, so this is not an essential requirement for the syndrome. The findings in these five cases suggest that the abnormal posturing associated with this syndrome may be the result of extreme sensitivity of the esophagus to refluxed gastric acid. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=511