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

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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Bibliographic Details
Main Authors: Ali Alsuheel Asseri, Ahmad Alzoani, Abdulwahab M. Almazkary, Nisreen Abdulaziz, Mufareh H. Almazkary, Samy Ailan Alahmari, Arul J. Duraisamy, Shruti Sureshkumar
Format: Article
Language:English
Published: MDPI AG 2023-04-01
Series:Diseases
Subjects:
MPS I
neonatal respiratory distress
pulmonary surfactant dysfunction
α-L-iduronidase
Online Access:https://www.mdpi.com/2079-9721/11/2/67

Internet

https://www.mdpi.com/2079-9721/11/2/67

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