Genetic Manifestations and Phenotype Spectrum in Infants With Feeding Difficulty

Genetic Manifestations and Phenotype Spectrum in Infants With Feeding Difficulty

ABSTRACT Background Feeding difficulties frequently co‐occur with multisystem disorders attributed to rare genetic diseases. In this study, we aimed to describe the genetic manifestations and phenotype spectrum in infants experiencing feeding difficulties. Methods This case series included infants u...

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Bibliographic Details
Main Authors: Mingyu Han, Wei Shi, Xiangxiang Chen, Dingwen Wu, Yi Sun, Weiyan Wang, Canyang Zhan, Lingling Hu, Tianming Yuan
Format: Article
Language:English
Published: Wiley 2024-08-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
clinical manifestations
feeding difficulty
multiple malformation
rare genetic disease
whole‐exome sequencing (WES)
Online Access:https://doi.org/10.1002/mgg3.70001
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https://doi.org/10.1002/mgg3.70001

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