| Literature DB >> 8113374 |
R P Stanton1, N Rao, C I Scott.
Abstract
de Barsy syndrome is a rare, genetically transmitted condition characterized by severe cutis laxa, joint hypermobility, growth retardation, mental retardation, and characteristic facies. Affected individuals have many orthopaedic manifestations, including developmental dysplasia of the hip, scoliosis, multiple joint dislocations and subluxations, and congenital vertical talus. The management of the orthopaedic manifestations of this syndrome is presented in two typical cases.Entities:
Mesh:
Year: 1994 PMID: 8113374 DOI: 10.1097/01241398-199401000-00013
Source DB: PubMed Journal: J Pediatr Orthop ISSN: 0271-6798 Impact factor: 2.324