Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review

ObjectiveTo share our experience on prenatal diagnosis of Williams-Beuren syndrome(WBS) and to improve the awareness, diagnosis, and intrauterine monitoring of the fetuses of this disease.MethodsThe study retrospectively evaluated 14 cases of WBS diagnosed prenatally by single nucleotide polymorphis...

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Bibliographic Details
Main Authors: Yunan Wang, Chang Liu, Rong Hu, Juan Geng, Jian Lu, Xianzhe Zhao, Ying Xiong, Jing Wu, Aihua Yin
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2023.1141665/full