Congenital Diaphragmatic Hernia as a Presentation of Mucopolysaccharidosis in a 3-year-old child: A Case Report

Background: Mucopolysaccharidoses (MPS) are rare, metabolic lysosomal storage disorders caused by the deficiency of enzymes required for the stepwise breakdown of glycosaminoglycans (GAGs). We report a case that was discovered to be Mucopolysaccharidosis Type II and was presented to the hospital wit...

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Detalles Bibliográficos
Autores principales: Al-Mashakbeh, Yazan, Heissat, Nizar, Al-Shaibei, Ahmad, Heissat, Nazek, Al-Faqeeh, Abdullah, Al-Jeady, Ahmad, Al Katatbeh, Mohammad, Khasawneh, Laith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iran University of Medical Sciences 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700400/
https://www.ncbi.nlm.nih.gov/pubmed/36447542
http://dx.doi.org/10.47176/mjiri.36.123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700400/
https://www.ncbi.nlm.nih.gov/pubmed/36447542
http://dx.doi.org/10.47176/mjiri.36.123

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