Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome

Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome

BackgroundSeveral studies have reported on the clinical phenotype of the 17q12 microduplication syndrome, a rare autosomal dominant genetic disorder, in children and adults, but few have reported on its prenatal diagnosis. This study analyzed the prenatal ultrasound phenotypes of the 17q12 microdupl...

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Bibliographic Details
Main Authors: Meiying Cai, Min Lin, Nan Guo, Meimei Fu, Liangpu Xu, Na Lin, Hailong Huang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Pediatrics
Subjects:
17q12 microduplication syndrome
fetal ultrasound phenotype
pregnancy outcome
chromosome microarray analysis
duodenal obstruction
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2022.910497/full

Internet

https://www.frontiersin.org/articles/10.3389/fped.2022.910497/full

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