Hunter syndrome with hyperthyroidism: a 16 month follow-up reprt
Mucopolysaccharidosis (MPS) is a rare genetic disorder caused by a deficiency in the activity of lysosomal enzymes required for glycosaminoglycan (GAG) degradation. An accumulation of GAG in many organs results in progressive cellular damage, and clinically results in joint stiffness, airway and car...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Indonesian Pediatric Society Publishing House,
2018-12-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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