The neonatal progeroid syndrome (Wiedemann-Rautenstrauch) and its relationship to Pelizaeus-Merzbacher's disease.

Détails

ID Serval
serval:BIB_A8894CCA5CE8
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
The neonatal progeroid syndrome (Wiedemann-Rautenstrauch) and its relationship to Pelizaeus-Merzbacher's disease.
Périodique
Neuropathology and Applied Neurobiology
Auteur⸱e⸱s
Ulrich J., Rudin C., Bubl R., Riederer B.M.
ISSN
0305-1846 (Print)
ISSN-L
0305-1846
Statut éditorial
Publié
Date de publication
1995
Volume
21
Numéro
2
Pages
116-120
Langue
anglais
Résumé
The neuropathology of a clinically well-documented case of the neonatal progeroid syndrome Wiedemann-Rautenstrauch is described. The most striking feature was a nearly complete absence of mature myelin in the brain. When immunohistochemistry for myelin basic protein was applied, some subcortical nerve fibres were accompanied by immature myelin sheaths. The neuropathology corresponds exactly to that of Pelizaeus-Merzbacher disease (Seitelberger type). Furthermore, this morphology, with the presence of myelin basic protein in the absence of mature myelin sheaths is reminiscent of the early stages of myelination in the newborn. From a brief review of the literature on Wiedemann-Rautenstrauch syndrome, we conclude, that the neuropathology of the syndrome is heterogeneous, and that there is relationship between the progeroid aspect and pathological myelination.
Mots-clé
Brain/pathology, Child, Demyelinating Diseases/metabolism, Diffuse Cerebral Sclerosis of Schilder/metabolism, Diffuse Cerebral Sclerosis of Schilder/pathology, Humans, Immunohistochemistry, Male, Myelin Sheath/metabolism, Syndrome
Pubmed
Web of science
Création de la notice
24/01/2008 15:34
Dernière modification de la notice
20/08/2019 16:13
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