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Arthrogryposis multiplex congenita

MONDO:0015168

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

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

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Sub-types

Arthrogryposis-renal dysfunction-cholestasis syndrome (1) Adducted thumbs-arthrogryposis syndrome, Christian type (0) Arthrogryposis due to muscular dystrophy (0) Arthrogryposis-hyperkeratosis syndrome, lethal form (0) Arthrogryposis-like syndrome (0) Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect (0) Arthrogryposis multiplex congenita 2, neurogenic type (0) Arthrogryposis multiplex congenita 3, myogenic type (0) Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum (0) Arthrogryposis multiplex congenita 5 (0) Arthrogryposis multiplex congenita 6 (0) Arthrogryposis multiplex congenita 7, X-linked (0) Arthrogryposis multiplex congenita-whistling face syndrome (0) Arthrogryposis, renal dysfunction, and cholestasis 1 (0) Arthrogryposis, renal dysfunction, and cholestasis 2 (0) Autosomal recessive myogenic arthrogryposis multiplex congenita (0) Fetal akinesia deformation sequence (0) Fetal akinesia deformation sequence 1 (0) Fetal akinesia deformation sequence 2 (0) Fetal akinesia deformation sequence 3 (0)

Broader categories

Disease (680) Hereditary disease (176) Human disease (14) Developmental defect during embryogenesis (8) Congenital limb malformation (3) Disease of genetic or genomic mechanism (2) Arthrogryposis syndrome (0) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of development or morphogenesis (0)
Not yet recruiting 1 Completed 2
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