Arora-Nirwane-Samant syndrome: A variant of Freeman-Sheldon syndrome

Abstract

Freeman-Sheldon syndrome (FSS) is a rare inherited form of distal arthrogryposis characterized by craniofacial abnormalities, camptodactyly with ulnar deviation of the fingers and talipes equinovarus. We present a case variant of FSS with proximal and distal arthrygryposis with the additional features of bilateral developmental dysplasia of the hip and bilateral congenital vertical talus deformity.