Dysostosis in mucopolysaccharidosis type 2: A case of longitudinal follow up and literature review

Mucopolysaccharidosis type 2 is a congenital lysosomal disease characterized by iduronate-2-sulfatase deficiency, which leads to excessive accumulation of glycosaminoglycans in tissue. Dysostosis, which primarily involves decreased bone mineralization with morphological changes in the bone, is a maj...

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Detalles Bibliográficos
Autores principales: Sasaki, Tomoaki, Ogata, Miki, Kajihama, Aya, Nakau, Kouichi, Okizaki, Atsutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809250/
https://www.ncbi.nlm.nih.gov/pubmed/33488893
http://dx.doi.org/10.1016/j.radcr.2021.01.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809250/
https://www.ncbi.nlm.nih.gov/pubmed/33488893
http://dx.doi.org/10.1016/j.radcr.2021.01.003

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