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Neurogenic arthrogryposis multiplex congenita

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Name:
Neurogenic arthrogryposis multiplex congenita
Description:
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy.
ORPHAcode:
1143
XREF(s):
Orphanet
MeSH
ICD-10
OMIM
Analyte(s):
SCYL2
COL25A1
ERGIC1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14