Freeman–Sheldon syndrome
| Freeman–Sheldon syndrome | |
|---|---|
| Other names | Distal arthrogryposis type 2A (DA2A), craniocarpotarsal dysplasia, craniocarpotarsal dystrophy, cranio-carpo-tarsal syndrome, whistling face–windmill vane hand syndrome |
| Specialty | Medical genetics |
Freeman–Sheldon syndrome (FSS) is a very rare form of multiple congenital contracture (MCC) syndromes (arthrogryposes) and is the most severe form of distal arthrogryposis (DA). It was originally described by Ernest Arthur Freeman and Joseph Harold Sheldon in 1938.: 577
As of 2007, only about 100 cases had been reported in medical literature.