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Alexander disease type I

Disease Export to PDF
Name:
Alexander disease type I
Description:
An astrogliopathy and the most severe and common form of Alexander disease (AxD), presenting before the age of 4 and characterized by seizures, megalencephaly and developmental delay with progressive deterioration.
ORPHAcode:
363717
Synonyms:
AxD type I
XREF(s):
Orphanet
OMIM
ICD-10
Analyte(s):
GFAP
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14