Arthrogryposis-severe scoliosis syndrome

Distal 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

1 clinical trial for this condition and its sub-types, 0 tagged with Arthrogryposis-severe scoliosis syndrome itself.