医学
静脉畸形
先天性畸形
皮肤病科
Klippel-Trenaunay综合征
血管畸形
基因检测
遗传综合征
病理
外科
儿科
内科学
软组织
遗传学
怀孕
生物
作者
Mollie Helena McMahon,Nasim Tahir,Meena Balasubramanian
出处
期刊:Case Reports
[BMJ]
日期:2022-06-01
卷期号:15 (6): e246114-e246114
标识
DOI:10.1136/bcr-2021-246114
摘要
Cutaneous venous malformations frequently present with blue-pink lesions on the skin or mucosal surfaces. They can be problematic for patients who experience pain or unsightly lesions and can also be associated with significant bleeding. A proportion of venous malformations have been noted to occur in families, in particular glomuvenous malformations (GVMs). A 'two-hit' occurrence of genetic pathogenic variants appears to explain the appearance of GVMs, with the initial change in the germline copy of GLMN followed by a second somatic hit. Here we discuss a report of siblings experiencing such lesions, which were diagnosed as GVMs by genetic testing. We include a review of the literature regarding the clinical and genetic differences between these groups of venous malformations.
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