Centre d'Information et de documentation du CRA Rhône-Alpes
CRA
Informations pratiques
-
Adresse
Centre d'information et de documentation
du CRA Rhône-Alpes
Centre Hospitalier le Vinatier
bât 211
95, Bd Pinel
69678 Bron CedexHoraires
Lundi au Vendredi
9h00-12h00 13h30-16h00Contact
Tél: +33(0)4 37 91 54 65
Mail
Fax: +33(0)4 37 91 54 37
-
Détail de l'auteur
Auteur Hanan COSTEFF |
Documents disponibles écrits par cet auteur (5)
Faire une suggestion Affiner la recherche
Biological factors in mild mental retardation / Hanan COSTEFF in Developmental Medicine & Child Neurology, 25-5 (October 1983)
[article]
Titre : Biological factors in mild mental retardation Type de document : Texte imprimé et/ou numérique Auteurs : Hanan COSTEFF, Auteur ; B. E. COHEN, Auteur ; L. E. WELLER, Auteur Année de publication : 1983 Article en page(s) : p.580-587 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A group of 434 children with non-syndromic mental retardation was analysed for frequency of recorded prenatal, perinatal and infantile biological disturbances. Mildly retarded individuals for unrelated parentage, both idiopathic and familial, had a strikingly higher prevalence of recorded disturbances than did a control group of retarded individuals with consanguineous parents and of probably genetic aetiology. These disturbances were as frequent among those with mild retardation as among parallel groups with severe retardation. The most significant single disturbance among the mildly retarded was a history of maternal reproductive inefficiency. These findings conflict with the view that mild retardation is predominantly 'cultural-familial' and is not pathological in nature. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=568
in Developmental Medicine & Child Neurology > 25-5 (October 1983) . - p.580-587[article] Biological factors in mild mental retardation [Texte imprimé et/ou numérique] / Hanan COSTEFF, Auteur ; B. E. COHEN, Auteur ; L. E. WELLER, Auteur . - 1983 . - p.580-587.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 25-5 (October 1983) . - p.580-587
Index. décimale : PER Périodiques Résumé : A group of 434 children with non-syndromic mental retardation was analysed for frequency of recorded prenatal, perinatal and infantile biological disturbances. Mildly retarded individuals for unrelated parentage, both idiopathic and familial, had a strikingly higher prevalence of recorded disturbances than did a control group of retarded individuals with consanguineous parents and of probably genetic aetiology. These disturbances were as frequent among those with mild retardation as among parallel groups with severe retardation. The most significant single disturbance among the mildly retarded was a history of maternal reproductive inefficiency. These findings conflict with the view that mild retardation is predominantly 'cultural-familial' and is not pathological in nature. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=568 Eye-Sighting Preference of Normal and Hemiplegic Children and Adults / Hanan COSTEFF in Developmental Medicine & Child Neurology, 30-3 (June 1988)
[article]
Titre : Eye-Sighting Preference of Normal and Hemiplegic Children and Adults Type de document : Texte imprimé et/ou numérique Auteurs : Hanan COSTEFF, Auteur ; Amikam RESHEF, Auteur ; Moe BERGMAN, Auteur ; Varda KOREN, Auteur ; Sara GREENBAUM, Auteur ; Malka ITZKOWITZ, Auteur ; Pablo SOLZI, Auteur Année de publication : 1988 Article en page(s) : p.360-364 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Préférence oculaire chez les enfants et adultes, normaux et hémiplégiques
La préférence oculaire a été examinée chez 32 enfants hémiplégiques, 51 patients hémiplegiques avec début à l'âge adulte, et 57 sujets normaux, enfants et adultes. La préférence oculaire a été comparée à la préférence auditive en écoute dichotique chez 25 des enfants hémiplégiques. Aucune association indépendante n'a pu être détectée entre la préférence oculaire et la préférence auditive. Chez l'enfant comme chez l'adulte hémiplégiques, la préférence oculaire se situait du même coté que l'hémisphère lésé. Chez l'adulte, cette tendance était plus prononcée en cas de lésions plus extensives, traduites par une aphasie et/ou une hémianopsie. Ces données sont interprétées comme une indication que à préférence oculaire n'est pas liée à une dominance hémisphérique unitaire et que, contrairement à l'audition et au langage, il n'y a pas d'irréversibilité aprés une période critique de développement. Une explication plus simple que la dominance hémisphérique incomplète est offerte par une association faiblement positive entre une latéralité croisée et un dysfonctionnement cérébral.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128
in Developmental Medicine & Child Neurology > 30-3 (June 1988) . - p.360-364[article] Eye-Sighting Preference of Normal and Hemiplegic Children and Adults [Texte imprimé et/ou numérique] / Hanan COSTEFF, Auteur ; Amikam RESHEF, Auteur ; Moe BERGMAN, Auteur ; Varda KOREN, Auteur ; Sara GREENBAUM, Auteur ; Malka ITZKOWITZ, Auteur ; Pablo SOLZI, Auteur . - 1988 . - p.360-364.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 30-3 (June 1988) . - p.360-364
Index. décimale : PER Périodiques Résumé : Préférence oculaire chez les enfants et adultes, normaux et hémiplégiques
La préférence oculaire a été examinée chez 32 enfants hémiplégiques, 51 patients hémiplegiques avec début à l'âge adulte, et 57 sujets normaux, enfants et adultes. La préférence oculaire a été comparée à la préférence auditive en écoute dichotique chez 25 des enfants hémiplégiques. Aucune association indépendante n'a pu être détectée entre la préférence oculaire et la préférence auditive. Chez l'enfant comme chez l'adulte hémiplégiques, la préférence oculaire se situait du même coté que l'hémisphère lésé. Chez l'adulte, cette tendance était plus prononcée en cas de lésions plus extensives, traduites par une aphasie et/ou une hémianopsie. Ces données sont interprétées comme une indication que à préférence oculaire n'est pas liée à une dominance hémisphérique unitaire et que, contrairement à l'audition et au langage, il n'y a pas d'irréversibilité aprés une période critique de développement. Une explication plus simple que la dominance hémisphérique incomplète est offerte par une association faiblement positive entre une latéralité croisée et un dysfonctionnement cérébral.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128 Pathogenic factors in idiopathic mental retardation / Hanan COSTEFF in Developmental Medicine & Child Neurology, 23-4 (August 1981)
[article]
Titre : Pathogenic factors in idiopathic mental retardation Type de document : Texte imprimé et/ou numérique Auteurs : Hanan COSTEFF, Auteur ; Bernard COHEN, Auteur ; Leonard WELLER, Auteur ; Howard KLECKNER, Auteur Année de publication : 1981 Article en page(s) : p.484-493 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Pathogenic factors in a mentally retarded population were evaluated by comparing their frequency among three groups of patients: a control group with predominantly genetic retardation and consanguineous parents; a group with severe idiopathic retardation and unrelated parents; and a group with mild idiopathic retardation and unrelated parents. Seven factors were found to be significantly more common among the patients with idiopathic retardation than in the genetic control group: a history of maternal reproductive inefficiency; bleeding during pregnancy; toxemia during pregnancy; signs of perinatal stress; neonatal anoxia; neonatal jaundice; and seizures during the first year of life. A history of repeated maternal abortions was particularly associated with mild retardation, and infantile seizures were particularly associated with severe retardation. The latter association remained significant even after exclusion of all infantile spasms, neonatal seizures and symptomatic seizures. Since the control group in this study was composed mainly of genetically retarded patients, the associations observed seem likely to be related to the causes of retardation rather than simply being the effects of a damaged fetus.
PIP: Several complications and diseases of pregnancy, delivery, and infancy have been found to be more prevalent among the mentally retarded than among normal children. In the course of reviewing 904 families of retarded children examined at the Tel Hashomer Assessment Center for the retarded (Israel), a group of 87 children with a nonspecific phenotype were isolated. Genetic analysis showed this to be of 75% autosomal recessive etiology. These mainly genetically retarded patients were used as a control group to assess a number of pathogenic factors in mental retardation. 3 groups of retarded patients with complete and reliable medical histories were compared: 87 retarded children with unidifferentiated phenotype, whose parents had normal intelligence and were either uncle-niece pairs or 1st cousins, and intelligence quotients (IQs) were less than 50 in 61 of these cases and between 50 and 69 in the remaining 26; 161 cases with idiopathic retardation with unrelated parents of normal intelligence, without retarded siblings; and 75 idiopathic retarded cases similar to the group of 161 cases but with only mild retardation. Complications of pregnancy, labor, and infancy were seen in 21 of the 61 control retarded groups with IQs under 50 and in 9 of the 26 with IQs 50 to 69. They were observed in 100 of the 161 cases of severe idiopathic retardation and in 53 of the 75 cases of mild idiopathic retardation. 11 factors were common enough to permit individual analysis: maternal age; history of multiple or recent spontaneous abortions; bleeding during pregnancy; toxemia; prematurity; low birthweight at term; signs of fetal or neonatal distress; neonatal anoxia; significant neonatal jaundice; convulsions during the 1st year of life; and evidence of early maternal neglect or chronic infantile illness. Maternal age over 35 at the time of birth was of no etiological importance. Abortions, either multiple or in the immediately preceding or subsequent pregnancy, were more than twice as common in the cases of mild idiopathic retardation as in the control group. The group with severe idiopathic retardation showed only a slight, insignificant increase in maternal abortions relative to the control group. Bleeding during early or middle pregnancy was more than 3 times as common in both the mild and severe idiopathic retarded groups as in the control group of homozygotes. Toxemia of pregnancy was twice as common among those with mild idiopathic retardation and 2-1/2 times as common in severe idiopathic retardation compared with the homozygote control group. Prematurity and low birthweight showed only a slight and nonsignificant rise in the 2 idiopathic groups relative to the controls. Signs of perinatal stress were practically nonexistent in the controls and were significantly more common in both the mild and severe idiopathic groups. Neonatal anoxia requiring some degree of medical attention was about 3 times as common in the 2 test groups. Events of neglect were as common in the control as in the other groups. Seizure prevalence in the 1st year of life showed a nonsignificant increase in the mild idiopathic group and an increase of marked significance in the severe idiopathic group relative to the controls.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=522
in Developmental Medicine & Child Neurology > 23-4 (August 1981) . - p.484-493[article] Pathogenic factors in idiopathic mental retardation [Texte imprimé et/ou numérique] / Hanan COSTEFF, Auteur ; Bernard COHEN, Auteur ; Leonard WELLER, Auteur ; Howard KLECKNER, Auteur . - 1981 . - p.484-493.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 23-4 (August 1981) . - p.484-493
Index. décimale : PER Périodiques Résumé : Pathogenic factors in a mentally retarded population were evaluated by comparing their frequency among three groups of patients: a control group with predominantly genetic retardation and consanguineous parents; a group with severe idiopathic retardation and unrelated parents; and a group with mild idiopathic retardation and unrelated parents. Seven factors were found to be significantly more common among the patients with idiopathic retardation than in the genetic control group: a history of maternal reproductive inefficiency; bleeding during pregnancy; toxemia during pregnancy; signs of perinatal stress; neonatal anoxia; neonatal jaundice; and seizures during the first year of life. A history of repeated maternal abortions was particularly associated with mild retardation, and infantile seizures were particularly associated with severe retardation. The latter association remained significant even after exclusion of all infantile spasms, neonatal seizures and symptomatic seizures. Since the control group in this study was composed mainly of genetically retarded patients, the associations observed seem likely to be related to the causes of retardation rather than simply being the effects of a damaged fetus.
PIP: Several complications and diseases of pregnancy, delivery, and infancy have been found to be more prevalent among the mentally retarded than among normal children. In the course of reviewing 904 families of retarded children examined at the Tel Hashomer Assessment Center for the retarded (Israel), a group of 87 children with a nonspecific phenotype were isolated. Genetic analysis showed this to be of 75% autosomal recessive etiology. These mainly genetically retarded patients were used as a control group to assess a number of pathogenic factors in mental retardation. 3 groups of retarded patients with complete and reliable medical histories were compared: 87 retarded children with unidifferentiated phenotype, whose parents had normal intelligence and were either uncle-niece pairs or 1st cousins, and intelligence quotients (IQs) were less than 50 in 61 of these cases and between 50 and 69 in the remaining 26; 161 cases with idiopathic retardation with unrelated parents of normal intelligence, without retarded siblings; and 75 idiopathic retarded cases similar to the group of 161 cases but with only mild retardation. Complications of pregnancy, labor, and infancy were seen in 21 of the 61 control retarded groups with IQs under 50 and in 9 of the 26 with IQs 50 to 69. They were observed in 100 of the 161 cases of severe idiopathic retardation and in 53 of the 75 cases of mild idiopathic retardation. 11 factors were common enough to permit individual analysis: maternal age; history of multiple or recent spontaneous abortions; bleeding during pregnancy; toxemia; prematurity; low birthweight at term; signs of fetal or neonatal distress; neonatal anoxia; significant neonatal jaundice; convulsions during the 1st year of life; and evidence of early maternal neglect or chronic infantile illness. Maternal age over 35 at the time of birth was of no etiological importance. Abortions, either multiple or in the immediately preceding or subsequent pregnancy, were more than twice as common in the cases of mild idiopathic retardation as in the control group. The group with severe idiopathic retardation showed only a slight, insignificant increase in maternal abortions relative to the control group. Bleeding during early or middle pregnancy was more than 3 times as common in both the mild and severe idiopathic retarded groups as in the control group of homozygotes. Toxemia of pregnancy was twice as common among those with mild idiopathic retardation and 2-1/2 times as common in severe idiopathic retardation compared with the homozygote control group. Prematurity and low birthweight showed only a slight and nonsignificant rise in the 2 idiopathic groups relative to the controls. Signs of perinatal stress were practically nonexistent in the controls and were significantly more common in both the mild and severe idiopathic groups. Neonatal anoxia requiring some degree of medical attention was about 3 times as common in the 2 test groups. Events of neglect were as common in the control as in the other groups. Seizure prevalence in the 1st year of life showed a nonsignificant increase in the mild idiopathic group and an increase of marked significance in the severe idiopathic group relative to the controls.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=522 Single-cause Attribution / Hanan COSTEFF in Developmental Medicine & Child Neurology, 30-3 (June 1988)
[article]
Titre : Single-cause Attribution Type de document : Texte imprimé et/ou numérique Auteurs : Hanan COSTEFF, Auteur Année de publication : 1988 Article en page(s) : p.410-412 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128
in Developmental Medicine & Child Neurology > 30-3 (June 1988) . - p.410-412[article] Single-cause Attribution [Texte imprimé et/ou numérique] / Hanan COSTEFF, Auteur . - 1988 . - p.410-412.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 30-3 (June 1988) . - p.410-412
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128 Vestibular Function of Hearing-impaired Children / Hanan COSTEFF in Developmental Medicine & Child Neurology, 30-4 (August 1988)
[article]
Titre : Vestibular Function of Hearing-impaired Children Type de document : Texte imprimé et/ou numérique Auteurs : Hanan COSTEFF, Auteur ; Michelle KORB, Auteur ; Hanna GREENGART, Auteur Année de publication : 1988 Article en page(s) : p.552-553 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128
in Developmental Medicine & Child Neurology > 30-4 (August 1988) . - p.552-553[article] Vestibular Function of Hearing-impaired Children [Texte imprimé et/ou numérique] / Hanan COSTEFF, Auteur ; Michelle KORB, Auteur ; Hanna GREENGART, Auteur . - 1988 . - p.552-553.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 30-4 (August 1988) . - p.552-553
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128