A Novel DNAH9 Gene Mutation Causing Primary Ciliary Dyskinesia With an Unusual Association of Jejunal Atresia in a Bahraini Child-Reference-Cited by-同舟云学术

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A Novel DNAH9 Gene Mutation Causing Primary Ciliary Dyskinesia With an Unusual Association of Jejunal Atresia in a Bahraini Child

Published:2022-12-26 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Isa Hasan M,Alkharsi Fatema A,Busehail Maryam Y,Haider Fayza

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference27 articles.

1. Kartagener's syndrome in 9 year old - a case report;Kansal S;Chest,2012

2. Liver transplantation in a child with Kartagener syndrome: a case report;Uludag Yanaral T;Int Med Case Rep J,2021

3. Medscape. primary ciliary dyskinesia (Kartagener syndrome). (2020). Accessed: December 9, 2022: https://emedicine.medscape.com/article/299299-overview.

4. Primary ciliary dyskinesia: An update on new diagnostic modalities and review of the literature;Popatia R;Pediatr Allergy Immunol Pulmonol,2014

5. Kartagener syndrome: a case report;Ibrahim R;Can J Respir Ther,2021

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1. Before an abducens palsy can be attributed to a congenital vitamin-B12 deficiency, alternative causes must be ruled out;Child's Nervous System;2023-07-14

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