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

Primary ciliary dyskinesia (PCD) is a rare autosomal recessive genetic disorder. It is caused by a defect in the action of the cilia lining multiple organs of the body, including the lungs, the sinuses, hepatobiliary and reproductive organs. In general, the estimated prevalence of this condition is...

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Detalles Bibliográficos
Autores principales: Isa, Hasan M, Alkharsi, Fatema A, Busehail, Maryam Y, Haider, Fayza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876387/
https://www.ncbi.nlm.nih.gov/pubmed/36712782
http://dx.doi.org/10.7759/cureus.32964

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9876387/
https://www.ncbi.nlm.nih.gov/pubmed/36712782
http://dx.doi.org/10.7759/cureus.32964

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