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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

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