Arthrogryposis-severe scoliosis syndrome
MONDO:0012195Distal arthrogryposis type 4 is an inherited developmental defect syndrome characterized by multiple congenital contractures of limbs, without primary neurologic and/or muscle disease that affects limb function, and a mild to severe scoliosis. Intelligence is normal.
Also known as: distal arthrogryposis type 4, distal arthrogryposis type IID, DA4, arthrogryposis with Severe scoliosis, arthrogryposis, distal, type 2D, arthrogryposis, distal, type 4
38 clinical trials for this condition and its sub-types.
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Disease
(618)
Musculoskeletal system disorder
(196)
Hereditary disease
(172)
Muscle tissue disorder
(53)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Arthrogryposis syndrome
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Disease by body system or component
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