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

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...

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Detalles Bibliográficos
Autores principales: Vasilevska, Lauma, Auzenbaha, Madara, Grinfelde, Ieva, Skangale, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424730/
https://www.ncbi.nlm.nih.gov/pubmed/36052356
http://dx.doi.org/10.3389/fped.2022.973193

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424730/
https://www.ncbi.nlm.nih.gov/pubmed/36052356
http://dx.doi.org/10.3389/fped.2022.973193

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