Gordon syndrome, or distal arthrogryposis type 3, is a rare genetic disorder characterized by cleft palate and congenital contractures of the hands and feet.

Other signs and symptoms include short stature, bifid uvula, hip dislocation, scoliosis or kyphosis, or syndactyly.

[1][2] Gordon syndrome is a rare autosomal dominant disorder caused by mutation in PIEZO2.

[2] It affects males and females equally.

This genetic disorder article is a stub.