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Mucopolysaccharidosis Type VI with Recurrent Chest Infection
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) is a progressive multi-systemic autosomal recessive disease resulting from a deficiency of arylsulfatase B (N-acetylgalactosamine-4-sulfatase). Here we report the case of a three-year-old male child born full-term via normal vaginal delivery. H...
Autores principales: | Numan, Ashraf, Alruwaili, Anoud N, Ali, Rehab, Alsharari, Hamasat, Alanazi, Mishal, Alazmi, Nouf N, Alsaati, Ahmed A |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032617/ https://www.ncbi.nlm.nih.gov/pubmed/36968901 http://dx.doi.org/10.7759/cureus.35229 |
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