Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Disrupted development of oropharyngeal structures as well as cranial nerve and brainstem circuits may lead to feeding and swallowing difficulties in children with 22q11. 2 deletion syndrome (22q11DS). We previously demonstrated aspiration-based dysphagia during early postnatal life in the LgDel mous...

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Bibliographic Details
Main Authors: Lauren Welby, Hailey Caudill, Gelila Yitsege, Ali Hamad, Filiz Bunyak, Irene E. Zohn, Thomas Maynard, Anthony-Samuel LaMantia, David Mendelowitz, Teresa E. Lever
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-01-01
Series:Frontiers in Neurology
Subjects:
22q11 deletion syndrome
DiGeorge syndrome
pediatric dysphagia
dysphagia
deglutition
feeding
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2020.00004/full

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https://www.frontiersin.org/article/10.3389/fneur.2020.00004/full

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