Larsen Syndrome Definition Terminology Encyclopedia Online
Larsen syndrome (LS) is a rare genetic disorder, with an incidence of about one in 100,000.
Larsen et al. called attention to a syndrome of multiple congenital dislocations and characteristic facies (prominent forehead, depressed nasal bridge, wide-spaced eyes).
Larsen syndrome is an osteochondrodysplasia characterized by large-joint dislocations and characteristic craniofacial abnormalities.
Larsen syndrome is a rare usually autosomal dominant congenital disorder that occurs in about every 1 in 100,000 people.