Case Report: First Case of Non-restrictive Ventricular Septal Defect With Congestive Heart Failure in a Chinese Han Male Infant Carrying a Class II Chromosome 17p13.3 Microduplication

Chromosome 17p13.3 microduplication syndrome is considered a multisystem disorder that results in a wide variety of clinical manifestations including dysmorphic facial characteristics, brain structural malformations, developmental restriction, growth restriction, and neurocognitive disorders. The tw...

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Bibliographic Details

Main Authors:	Yung-Yu Yang, Chun-Ting Liu, Li-Fan Pai, Chih-Fen Hu, Shyi-Jou Chen, Wan-Fu Hsu
Format:	Artigo
Language:	Inglês
Published:	Frontiers Media S.A. 2022-02-01
Series:	Frontiers in Pediatrics
Subjects:	congenital heart disease congestive heart failure chromosome 17p13.3 microduplication microarray comparative genomic hybridization ventricular septal defect
Online Access:	https://www.frontiersin.org/articles/10.3389/fped.2022.825298/full
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