Volume 16, Issue 56 (Jan 2007)                   J Mazandaran Univ Med Sci 2007, 16(56): 136-142 | Back to browse issues page

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Mojtahedzadeh F, Rashidi ghader F, Alaee A, Tale A. Mucopoly saccharidosis type maroteaux-lamy, a case report. J Mazandaran Univ Med Sci. 2007; 16 (56) :136-142
URL: http://jmums.mazums.ac.ir/article-1-188-en.html
Abstract:   (24990 Views)
Mucopolysaccharidosis type maroteaux-lamy is a very rare hereditary disease. The disease is marked by the deficiency of the lysosomal enzyme N-Acetyl galactosamine-a-4-sulfate sulfatase (arylsulfatase B). It is inherited as an autosomal recessive trait. The most clinical manifestations are: corneal clouding, organomegaly, hernias, coarse facial features, cardiac insufficiency and skeletal abnormalities (dysostosis multiplex). The mental performance remains relatively normal. This is a case report of a child with clinical manifestations of mucopolysaccharidosis type maroteaux-lamy.
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Type of Study: Research(Original) |

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