A case report of a patient with mucopolysaccharidosis type II
Mucopolysaccharidosis type II (MPS II) or Hunter syndrome is an inborn error of metabolism due to lysosomal accumulation, with a recessive inheritance pattern linked to the X chromosome. It is caused by a deficiency in the activity of the lysosomal enzyme iduronate-2-sulfatase encoded by the IDS gen...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Permanyer
2017-04-01
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| Series: | Revista Médica del Hospital General de México |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S0185106316300853 |