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.

Also known as: arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome, distal arthrogryposis type 5, distal arthrogryposis type IIB, distal arthrogryposis with ophthalmoplegia, oculomelic amyoplasia, Arthogryposis with oculomotor limitation and electroretinal abnormalities, DA5, arthrogryposis ophthalmoplegia retinopathy

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