A Case Report of Mucopolysaccharidosis Type VI
BACKGROUND AND OBJECTIVE: Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disorder and autosomal recessive caused by arylsulfatase B deficiency in the body and progressive accumulation of glycosaminoglycan in different organs. Considering that this disease has low prevalence in Iran an...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Babol University of Medical Sciences
2018-12-01
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| Series: | Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul |
| Subjects: | |
| Online Access: | http://jbums.org/browse.php?a_code=A-10-4313-1&slc_lang=en&sid=1 |