Mucopoly saccharidosis type maroteaux-lamy, a case report

AbstractMucopolysaccharidosis type maroteaux-lamy is a very rare hereditary disease. The disease is marked by the deficiency of the lysosomal enzyme N-Acetyl galactosamine--4-sulfate sulfatase (arylsulfatase B). It is inherited as an autosomal recessive trait. The most clinical manifestations are:...

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Bibliografski detalji

Glavni autori:	A.R. Alaee, F. Rashidi ghader, F. Mojtahedzadeh, A. Tale
Format:	Artigo
Jezik:	Inglês
Izdano:	Mazandaran University of Medical Sciences 2007-01-01
Serija:	Journal of Mazandaran University of Medical Sciences
Teme:	Metabolic disorders mucopolysaccharidosis type maroteaux-lamy
Online pristup:	http://www.mazums.ac.ir/files/onlineJournals_2398818=mojtahedzadeh.pdf
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