Mucopolysaccharidosis Type I Presenting with Persistent Neonatal Respiratory Distress: A Case Report

Mucopolysaccharidosis type I (MPS I) is a rare inherited autosomal recessive lysosomal storage disorder. Despite several reports on MPS I-related neonatal interstitial lung disease, it is still considered to be an under-recognized disease manifestation. Thus, further study of MPS I is required to im...

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Detalles Bibliográficos
Autores principales: Asseri, Ali Alsuheel, Alzoani, Ahmad, Almazkary, Abdulwahab M., Abdulaziz, Nisreen, Almazkary, Mufareh H., Alahmari, Samy Ailan, Duraisamy, Arul J., Sureshkumar, Shruti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204566/
https://www.ncbi.nlm.nih.gov/pubmed/37218880
http://dx.doi.org/10.3390/diseases11020067

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