A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family.

ABSTRACT:

Objective

Tricuspid atresia (TA) is a rare life-threatening form of congenital heart defect (CHD). The genetic mechanisms underlying TA are not clearly understood. According to previous studies, the endocardial cushioning event, as the primary sign of cardiac valvulogenesis, is governed by several overlapping signaling pathways including Ras/ ERK pathway. RASA1, a regulator of cardiovascular development, is involved in this pathway and its haploinsufficiency (due to heterozygous mutations) has been identified as the underlying etiology of the autosomal dominant capillary malformation/arteriovenous malformation (CM/AVM).

Materials and methods

In this prospective study, we used whole exome sequencing (WES) followed by serial bioinformatics filtering steps for two siblings with

SUBMITTER: Nozari A 

PROVIDER: S-EPMC6275424 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature