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Up to: Distal arthrogryposis
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome
Distal arthrogryposis type 5 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 ocular anomalies (ptosis, external ophtalmoplegia and/or strabismus). Intelligence is normal.
This condition has no sub-types.