Congenital muscular dystrophy with cerebellar involvement

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Name:
Congenital muscular dystrophy with cerebellar involvement
Description:
A rare, congenital muscular dystrophy due to dystroglycanopathy characterized by proximal muscle weakness with a tendency for muscle hypertrophy and pseudohypertrophy, variable cognitive impairment, microcephaly, cerebellar hypoplasia with or without cysts, and other structural brain anomalies.
ORPHAcode:
370959
Synonyms:
CMD with cerebellar involvement
CMD-CRB
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14