arthrogryposis multiplex congenita
MONDO:0015168Also known as: AMC, Arthromyodysplasia congenita, arthrogryposis multiplex congenita, congenital arthromyodysplasia, multiple congenital arthrogryposis
- MONDO:
- MONDO:0015168
- Orphanet:
- 1037 ↗
Rare disease43 associated genes
Description
Arthrogryposis multiplex congenita (AMC) is a group of disorders characterized by congenital limb contractures. It manifests as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. AMC is always associated with decreased intrauterine fetal movement which leads secondarily to the contractures.
Associated genes
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