Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) in the pre-Columbian culture of Colombia

Mucopolysaccharidosis type VI or Maroteaux Lamy syndrome is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B, the clinical features include short stature, hepatosplenomegaly, dysostosis multiplex, stiff joints, corneal clouding, cardiac abnormalities,...

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Detalles Bibliográficos
Autores principales: Pachajoa, Harry, Rodriguez, Carlos Armando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Universidad del Valle 2014
Materias:
Windows To History
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123588/
https://www.ncbi.nlm.nih.gov/pubmed/25100895

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123588/
https://www.ncbi.nlm.nih.gov/pubmed/25100895

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