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Auteur Clive HARPER |
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Proliferative vasculopathy and an hydranencephalic-hydrocephalic syndrome: a neuropathological study of two siblings / Clive HARPER in Developmental Medicine & Child Neurology, 25-2 (April 1983)
[article]
Titre : Proliferative vasculopathy and an hydranencephalic-hydrocephalic syndrome: a neuropathological study of two siblings Type de document : Texte imprimé et/ou numérique Auteurs : Clive HARPER, Auteur ; Athel HOCKEY, Auteur Année de publication : 1983 Article en page(s) : p.232-239 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Two female siblings were born with an hydranencephalic-hydrocephalic syndrome, following pregnancies complicated by hydramnios. No environmental factors such as infections, drugs or metabolic disorders were noted during either pregnancy. Neuropathological studies revealed identical changes in each case. The characteristic feature of the pathology was a proliferative vasculopathy throughout the central nervous system, which apparently caused focal ischaemic lesions and progressive destruction of CNS tissue. The defect probably is inherited as an autosomal recessive trait. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=561
in Developmental Medicine & Child Neurology > 25-2 (April 1983) . - p.232-239[article] Proliferative vasculopathy and an hydranencephalic-hydrocephalic syndrome: a neuropathological study of two siblings [Texte imprimé et/ou numérique] / Clive HARPER, Auteur ; Athel HOCKEY, Auteur . - 1983 . - p.232-239.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 25-2 (April 1983) . - p.232-239
Index. décimale : PER Périodiques Résumé : Two female siblings were born with an hydranencephalic-hydrocephalic syndrome, following pregnancies complicated by hydramnios. No environmental factors such as infections, drugs or metabolic disorders were noted during either pregnancy. Neuropathological studies revealed identical changes in each case. The characteristic feature of the pathology was a proliferative vasculopathy throughout the central nervous system, which apparently caused focal ischaemic lesions and progressive destruction of CNS tissue. The defect probably is inherited as an autosomal recessive trait. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=561