Hurler Syndrome (Mucopolysaccharidosis Type 1): A Case Report

Hurler syndrome is a rare autosomal recessive disorder of deficiency in the metabolism of glycosaminoglycans (GAGs), including heparan sulfate and dermatan sulfate, which consequently accumulate in the different organs of the body, resulting from deficiency of an enzyme named Alpha-L-iduronidase. He...

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Detalles Bibliográficos
Autores principales: Khalid, Noman, Abdullah, Muhammad, Awais, Abeer bin, Hassan, Muhammad, Muhammad, Ameer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195038/
https://www.ncbi.nlm.nih.gov/pubmed/37213966
http://dx.doi.org/10.7759/cureus.37785

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10195038/
https://www.ncbi.nlm.nih.gov/pubmed/37213966
http://dx.doi.org/10.7759/cureus.37785

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