MUCOPOLY SACCHARIDOSIS TYPE MAROTEAUX-LAMY, A CASE REPORT

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MOJTAHEDZADEH F.; RASHIDI GHADER F.; ALAEI A.; TALE A.

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Journal Paper

Paper Information

Journal: Journal of Mazandaran University of Medical Sciences Year:2007 | Volume:16 | Issue:56 Page(s): 136-142

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Title

MUCOPOLY SACCHARIDOSIS TYPE MAROTEAUX-LAMY, A CASE REPORT

Author(s)

MOJTAHEDZADEH F. | RASHIDI GHADER F. | ALAEI A. | TALE A. | Issue Writer Certificate

Keywords

METABOLIC DISORDERSQ2

MUCOPOLYSACCHARIDOSIS TYPE MAROTEAUX-LAMYQ3

Abstract

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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APA: Copy

MOJTAHEDZADEH, F., RASHIDI GHADER, F., ALAEI, A., & TALE, A.. (2007). MUCOPOLY SACCHARIDOSIS TYPE MAROTEAUX-LAMY, A CASE REPORT. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 16(56), 136-142. SID. https://sid.ir/paper/45641/en

Vancouver: Copy

MOJTAHEDZADEH F., RASHIDI GHADER F., ALAEI A., TALE A.. MUCOPOLY SACCHARIDOSIS TYPE MAROTEAUX-LAMY, A CASE REPORT. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2007;16(56):136-142. Available from: https://sid.ir/paper/45641/en

IEEE: Copy

F. MOJTAHEDZADEH, F. RASHIDI GHADER, A. ALAEI, and A. TALE, “MUCOPOLY SACCHARIDOSIS TYPE MAROTEAUX-LAMY, A CASE REPORT,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 16, no. 56, pp. 136–142, 2007, [Online]. Available: https://sid.ir/paper/45641/en

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