Updates in Advances in Therapeutic Options for Pulmonary and Sleep Disorders in Mucopolysaccharidosis (MPS) Patients: A Narrative Review

Abstract excerpt

Mucopolysaccharidosis (MPS) are a group of inherited lysosomal storage genetic disorders that affect the body's ability to break down glycosaminoglycans (GAGs) due to the deficiency of required enzymes. This leads to depositions of these GAGs in various tissues and organs resulting in multi-systemic manifestations including pulmonary and sleep related issues. In recent years, there have been significant advancemen...

Topics

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• Carbohydrate Chemistry and Synthesis
• Disease Models, Animal
• Early Diagnosis
• Iduronidase
• Lysosomal Storage Disorders Research
• Mucopolysaccharidosis I
• Phenotype
• Proteoglycans and glycosaminoglycans research

Identifiers and source

Literature Corpus work

3086028c-2500-5045-b9fc-a089fa078927

DOI

10.20944/preprints202604.1101.v1