Gordon syndrome

An extremely rare multiple congenital malformation syndrome characterized by congenital contractures of hand and feet with variable degrees of severity of camptodactyly, clubfoot and, less frequently, cleft palate. Intelligence is normal but in some cases, additional abnormalities, such as short stature, kyphoscoliosis, ptosis, micrognathia, and cryptorchidism may also be present. Gordon syndrome, Marden-Walker syndrome and arthrogryposis with oculomotor limitation and electroretinal anomalies clinically and genetically overlap, and could represent variable expressions of the same condition.

Also known as: Gordon syndrome, camptodactyly-cleft palate-clubfoot syndrome, distal arthrogryposis type 3, distal arthrogryposis type IIA, DA3, arthrogryposis distal type 3, arthrogryposis multiplex congenita, distal, type 2A, arthrogryposis, distal, type 3

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