| Literature DB >> 20731866 |
Matthew Salter1, Chandoo Kalmat, Henry Kroll, David Kim.
Abstract
The Marshall Smith Syndrome (MSS) is a rare congenital disorder, displaying a constellation of unique symptoms, including orofacial dysmorphisms, accelerated osseous maturation and dysplasias, mental retardation, and respiratory maladies. Few individuals with MSS survive past early childhood. In this case report, we describe a unique treatment for a 30 year-old patient with MSS who presented to our pain medicine clinic for management of pain secondary to uncontrolled bilateral hip dysplasias.Entities:
Year: 2010 PMID: 20731866 PMCID: PMC2933713 DOI: 10.1186/1749-799X-5-61
Source DB: PubMed Journal: J Orthop Surg Res ISSN: 1749-799X Impact factor: 2.359