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...

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Detalles Bibliográficos
Autores principales: Numan, Ashraf, Alruwaili, Anoud N, Ali, Rehab, Alsharari, Hamasat, Alanazi, Mishal, Alazmi, Nouf N, Alsaati, Ahmed A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
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

Internet

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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