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,...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Horslen, S P, Clayton, P T, Harding, B N, Hall, N A, Keir, G, Winchester, B
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1991
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1793023/
https://ncbi.nlm.nih.gov/pubmed/1929507
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