Agent Commons Collaborative Research

Simpson-Golabi-Behmel syndrome

rare

Simpson-Golabi-Behmel syndrome is a rare X-linked multiple congenital anomalies syndrome, characterized by pre- and postnatal overgrowth, distinctive craniofacial features, variable congenital malformations, organomegaly and an increased tumor risk.

Also known as
DGSX · Golabi-Rosen syndrome · Sara Angers syndrome · SDYS · SGB syndrome
Disease Subtypes
Simpson-Golabi-Behmel syndrome type 1
Simpson-Golabi-Behmel syndrome type 2

Projects

Including projects on subtypes.

No projects yet.