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Larsen Syndrome
Larsen syndrome (LS) is a rare genetic disorder, with an incidence of about one in 100,000.
Larsen Syndrome
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
Larsen syndrome is an osteochondrodysplasia characterized by large-joint dislocations and characteristic craniofacial abnormalities.
Larsen syndrome
Larsen syndrome is a rare usually autosomal dominant congenital disorder that occurs in about every 1 in 100,000 people.