A GENE FOR FAMILIAL VENOUS MALFORMATIONS MAPS TO CHROMOSOME-9P IN A 2ND LARGE KINDRED

被引:106
作者
GALLIONE, CJ
PASYK, KA
BOON, LM
LENNON, F
JOHNSON, DW
HELMBOLD, EA
MARKEL, DS
VIKKULA, M
MULLIKEN, JB
WARMAN, ML
PERICAKVANCE, MA
MARCHUK, DA
机构
[1] DUKE UNIV,DEPT GENET,DURHAM,NC 27710
[2] UNIV MICHIGAN,INST GERONTOL,ANN ARBOR,MI 48109
[3] HARVARD UNIV,CHILDRENS HOSP,SCH MED,DIV PLAST SURG,BOSTON,MA 02115
[4] DUKE UNIV,SCH MED,DIV NEUROL,DURHAM,NC 27710
[5] UNIV MICHIGAN,SCH MED,CTR HUMAN GENOME,FAMILY STUDIES CORE,ANN ARBOR,MI 48109
[6] HARVARD UNIV,SCH MED,DEPT CELL BIOL,BOSTON,MA 02115
关键词
D O I
10.1136/jmg.32.3.197
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Venous malformations are a common farm 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.
引用
收藏
页码:197 / 199
页数:3
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