Arthrogryposis multiplex congenita

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.

Also known as: AMC, Arthromyodysplasia congenita, arthrogryposis multiplex congenita, congenital arthromyodysplasia, multiple congenital arthrogryposis, myodysplasia, Guerin-Stern syndrome, Guérin-Stern syndrome

6 clinical trials for this condition and its sub-types.