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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,...
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| Опубликовано в: : | Colombia Médica |
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| Главные авторы: | , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Universidad del Valle
2014
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| Предметы: | |
| Online-ссылка: | 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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