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Up to: Hereditary disease · Arthrogryposis syndrome
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.
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Arthrogryposis multiplex congenita 2, neurogenic type 0 trials · 1 incl. sub-types Sub-types →
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Marden-Walker syndrome 0 trials
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Arthrogryposis multiplex congenita 5 0 trials
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Arthrogryposis multiplex congenita 6 0 trials
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Arthrogryposis-like syndrome 0 trials
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Van den Ende-Gupta syndrome 0 trials