Larsen syndrome, autosomal dominant
Larsen syndrome, autosomal dominant
A genetically heterogeneous disorder (OMIM:150250) characterised by multiple joint dislocations, with equinovarus or equinovalgus foot deformities, craniofacial defects (hypertelorism, prominence of the forehead, a depressed nasal bridge and a flattened midface) and accessory carpal bones.Molecular pathology
Defects in FLNB, which encodes filamin B, cause Larsen syndrome.