Work

A gene for familial venous malformations maps to chromosome 9p in a second large kindred.

Year: 1995
Type: article
Study design: Observational Study
Abstract: Venous malformations are a common form of vascular anomaly that cause pain and disfigurement and can be life threatening if they involve critical organs. They occur sporadically or in a familial form, where multiple lesions are usually present. We have identified a large kindred showing autosomal dominant inheritance of venous malformations. Using this family we confirm linkage of a familial form of venous malformations to chromosome 9p. We suggest that blue rubber bleb naevus syndrome can be considered a particular manifestation of this form of familial venous malformations. The candidate region for this gene encompasses the interferon gene cluster and the MTS1 (p16) tumour suppressor gene.
Language: English
Subfield: Surgery
Field: Medicine
Open Access status: bronze
OpenAlex ID: W1984098940
FWCI: 3.014
Cites: 15
Cited by: 151
Related to: 10