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Mucopolysaccharidosis Type I Presenting with Persistent Neonatal Respiratory Distress: A Case Report
Autor:
Ali Alsuheel Asseri, Ahmad Alzoani, Abdulwahab M. Almazkary, Nisreen Abdulaziz, Mufareh H. Almazkary, Samy Ailan Alahmari, Arul J. Duraisamy, Shruti Sureshkumar
Publikováno v:
Diseases, Vol 11, Iss 2, p 67 (2023)
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 manifestati
Externí odkaz:
https://doaj.org/article/e802cf3140bc437fbcd8b482146fbd17
