| Literature DB >> 26135202 |
Daniel Gutierrez1, Kevin D Cooper2, Anna L Mitchell3, Heather I Cohn2.
Abstract
Buschke-Ollendorff syndrome is a rare autosomal dominant disorder caused by loss of function in LEMD3, resulting in connective tissue nevi and varying bone dysplasia. Although typically benign, we describe a novel LEMD3 splice site mutation (IVS12 + 1delG) in a 13-year-old boy with Buschke-Ollendorff syndrome presenting with severe skeletal deformities, polyostotic melorheostosis, and osteopoikilosis.Entities:
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Year: 2015 PMID: 26135202 DOI: 10.1111/pde.12634
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588