The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

Aicardi-Goutières syndrome (Mendelian inheritance in man Catalog No *225750) is an autosomal recessive encephalopathy which causes developmental arrest, intracerebral calcification, and white matter disease in the presence of chronic cerebrospinal fluid lymphocytosis, and a raised level of cerebrosp...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Tolmie, J L, Shillito, P, Hughes-Benzie, R, Stephenson, J B
Format: Artigo
Sprog:Inglês
Udgivet: 1995
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051740/
https://ncbi.nlm.nih.gov/pubmed/8592332
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker