Treatment of latent tuberculosis in a child with mucopolysaccharidosis type I receiving enzyme replacement therapy: A case report

• Autori principali: Lauma Vasilevska (Autore), Madara Auzenbaha (Autore), Ieva Grinfelde (Autore), Anita Skangale (Autore)
• Natura: Libro
• Pubblicazione: Frontiers Media S.A., 2022-08-01T00:00:00Z.
• Soggetti: article
• Accesso online: Connect to this object online.

Mucopolysaccharidosis type I S (MPS IS) is a rare autosomal recessive lysosomal storage disorder caused by mutations in the IDUA gene, leading to a deficiency of the enzyme alpha-L-iduronidase. Enzyme replacement therapy (ERT) reduces lysosomal storage in the liver and improves clinical manifestatio...