Lissencephaly type 1 due to doublecortin gene mutation

Disease Export to PDF
Name:
Lissencephaly type 1 due to doublecortin gene mutation
Description:
Type 1 lissencephaly due to doublecortin (DCX) gene mutations is a semi-dominant X-linked disease characterised by intellectual deficiency and seizures that are more severe in male patients.
ORPHAcode:
2148
Synonyms:
X-linked lissencephaly type 1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14