Pontocerebellar hypoplasia type 1

Disease Export to PDF
Name:
Pontocerebellar hypoplasia type 1
Description:
A severe, genetic form of pontocerebellar hypoplasia (PCH) characterized by spinal cord anterior horn cell degeneration in addition to pontocerebellar hypoplasia. Clinically, patients manifest with a severe global development deficit that is evident early on from difficulties in feeding and swallowing
ORPHAcode:
2254
Synonyms:
Norman disease
PCH1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14