Total Hip Arthroplasty in a Patient with Mucopolysaccharidosis Type IVB

Introduction. Morquio syndrome or mucopolysaccharidosis (MPS) type IV is a rare autosomal recessive lysosomal storage disease, characterized by abnormal metabolism of glycosaminoglycans associated with specific skeletal deformities, also known as dysostosis multiplex. Case Presentation. We present t...

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Detalles Bibliográficos
Autores principales: van den Eeden, Yannick N. T., Unter Ecker, Niklas, Kleinertz, Holger, Gehrke, Thorsten, Ballhause, Tobias M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102130/
https://www.ncbi.nlm.nih.gov/pubmed/34012686
http://dx.doi.org/10.1155/2021/5584408

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102130/
https://www.ncbi.nlm.nih.gov/pubmed/34012686
http://dx.doi.org/10.1155/2021/5584408

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