Mucopolysaccharidosis type VI
This type is also called Maroteaux-Lamy syndrome and multiple dystrophic dwarfism. It is also an autosomal recessive hereditary disease. It is characterized by short stature, corneal opacity, but normal intelligence. This type of mucopolysaccharidosis was first discovered by Maroteaux (1963) and is an independent disease different from other types of mucopolysaccharidosis.
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Site of disease:
whole body -
Infectious :
Not contagious -
Frequent population:
child -
Related symptoms:
Muscle contracture abnormal short stature abnormal body shape abnormal short stature short neck -
Concurrent disease:
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Manufacturer:
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Palm chloramphenicol (type B) tablets
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Manufacturer:
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