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Article

Identification and Molecular Characterization of a <i>de novo</i> Supernumerary Ring Chromosome 18 in a Patient with Klippel‐Trenaunay Syndrome

28 Jun 2004

Abstract excerpt

Klippel-Trenaunay syndrome (KTS) is a congenital vascular disorder comprised of capillary, venous and lymphatic malformations associated with overgrowth of the affected tissues. In this study, we report the identification of a de novo supernumerary ring chromosome in a patient with mild mental retardation, long tapering fingers, elongated, thin feet and Klippel-Trenaunay syndrome (KTS). The ring marker chromosome...

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PMID: 15225160
DOI: 10.1046/j.1529-8817.2004.00095.x

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