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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Detalles Bibliográficos
Autores principales: Yang, Yung-Yu, Liu, Chun-Ting, Pai, Li-Fan, Hu, Chih-Fen, Chen, Shyi-Jou, Hsu, Wan-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926061/
https://www.ncbi.nlm.nih.gov/pubmed/35311053
http://dx.doi.org/10.3389/fped.2022.825298

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926061/
https://www.ncbi.nlm.nih.gov/pubmed/35311053
http://dx.doi.org/10.3389/fped.2022.825298

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