Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet rare-disease nomenclature term Orphanet_1154) can be described as follows. 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: Distal arthrogryposis type 5, Distal arthrogryposis type IIB, Distal arthrogryposis with ophthalmoplegia, Oculomelic amyoplasia.