Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome.

Two brothers presented with olivopontocerebellar atrophy of neonatal onset. The clinical features (failure to thrive, hypotonia, liver disease, effusions, and visual inattention) were similar to those of the four cases already reported, as were the necropsy findings of olivopontocerebellar atrophy,...

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Bibliografski detalji
Glavni autori: Horslen, S P, Clayton, P T, Harding, B N, Hall, N A, Keir, G, Winchester, B
Format: Artigo
Jezik:Inglês
Izdano: 1991
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1793023/
https://ncbi.nlm.nih.gov/pubmed/1929507
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