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Mucopolysaccharidosis type I Hurler-Scheie syndrome: A rare case report

Mucopolysaccharidosis I (MPS I) is a rare inherited disorder that belongs to a group of clinically progressive disorders and is caused by the deficiency of the lysosomal enzyme, α(1)-iduronidase. MPS I has been recently classified into a severe (Hurler syndrome) and an attenuated type (Hurler-Scheie...

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Detalles Bibliográficos
Autores principales:	Tatapudi, Ramesh, Gunashekhar, M., Raju, P. Suryanarayana
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications Pvt Ltd 2011
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220181/ https://www.ncbi.nlm.nih.gov/pubmed/22114460 http://dx.doi.org/10.4103/0976-237X.79287

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