Mucopolysaccharidosis type VI: a cardiologist's guide to diagnosis and treatment.

  title={Mucopolysaccharidosis type VI: a cardiologist's guide to diagnosis and treatment.},
  author={Adam Golda and Agnieszka Jurecka and Violetta Opoka-Winiarska and Anna Tylki-Szymańska},
  journal={International journal of cardiology},
  volume={167 1},
Mucopolysaccharidosis type VI (MPS VI, Maroteaux-Lamy syndrome) is an inborn error of metabolism, with incidences at birth ranging from 1 in 1.5 million to 1 in 43,000 live births. This disorder is rarely considered when evaluating patients with common populational cardiovascular diseases. A significant number of MPS VI patients, however, do present cardiovascular disease and MPS VI should be considered as a potential differential diagnosis for other cardiovascular disorders. This article… CONTINUE READING
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