A Primer on a Comprehensive Genetic Approach to Vascular Anomalies

被引:30
作者
Borst, Alexandra J. [1 ]
Nakano, Taizo A. [2 ]
Blei, Francine [3 ]
Adams, Denise M. [4 ]
Duis, Jessica [2 ]
机构
[1] Vanderbilt Univ, Med Ctr, Vasc Anomalies Program, Monroe Carrell Jr Childrens Hosp, Nashville, TN 37235 USA
[2] Univ Colorado, Sch Med, Vasc Anomalies Ctr, Childrens Hosp Colorado, Aurora, CO 80045 USA
[3] Northwell Hlth, Vasc Anomalies Program, Lenox Hill Hosp, New York, NY USA
[4] Univ Penn, Childrens Hosp Philadelphia, Vasc Anomalies Ctr, Philadelphia, PA 19104 USA
来源
FRONTIERS IN PEDIATRICS | 2020年 / 8卷
关键词
vascular malformations; genetic; mutation; anomalies; somatic; MOSAIC ACTIVATING MUTATIONS; VENOUS MALFORMATION; SOMATIC MUTATIONS; SIROLIMUS; HEMANGIOMAS; OVERGROWTH; DISORDERS; GERMLINE; SPECTRUM; GNAQ;
D O I
10.3389/fped.2020.579591
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The field of vascular anomalies has grown tremendously in the last few decades with the identification of key molecular pathways and genetic mutations that drive the formation and progression of vascular anomalies. Understanding these pathways is critical for the classification of vascular anomalies, patient care, and development of novel therapeutics. The goal of this review is to provide a basic understanding of the classification of vascular anomalies and knowledge of their underlying molecular pathways. Here we provide an organizational framework for phenotype/genotype correlation and subsequent development of a diagnostic and treatment roadmap. With the increasing importance of genetics in the diagnosis and treatment of vascular anomalies, we highlight the importance of clinical geneticists as part of a comprehensive multidisciplinary vascular anomalies team.
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页数:19
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