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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,...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Pachajoa, Harry, Rodriguez, Carlos Armando
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Universidad del Valle 2014
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4123588/
https://ncbi.nlm.nih.gov/pubmed/25100895
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