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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,...
Gardado en:
| Publicado en: | Colombia Médica |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Universidad del Valle
2014
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| Assuntos: | |
| Acceso en liña: | https://www.redalyc.org/articulo.oa?id=28331323008 https://www.redalyc.org/journal/283/28331323008/ https://www.redalyc.org/journal/283/28331323008/html/ https://www.redalyc.org/journal/283/28331323008/28331323008.epub https://www.redalyc.org/journal/283/28331323008/movil |
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