| Literature DB >> 17963221 |
Julie C Sapp1, Joyce T Turner, Jiddeke M van de Kamp, Fleur S van Dijk, R Brian Lowry, Leslie G Biesecker.
Abstract
We present a series of seven patients who were previously diagnosed with Proteus syndrome, but who do not meet published diagnostic criteria for this disorder and whose natural history is distinct from that of Proteus syndrome. This newly recognized phenotype comprises progressive, complex, and mixed truncal vascular malformations, dysregulated adipose tissue, varying degrees of scoliosis, and enlarged bony structures without progressive bony overgrowth. We have named this condition congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) on a heuristic basis. In contrast to the bony distortion so characteristic of Proteus syndrome, distortion in CLOVE syndrome occurs only following major or radical surgery. Here, we contrast differences and similarities of CLOVE syndrome to Proteus syndrome. (c) 2007 Wiley-Liss, Inc.Entities:
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Year: 2007 PMID: 17963221 DOI: 10.1002/ajmg.a.32023
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802