Mucopolysaccharidosis Type 3B in an Adult with Pancytopenia: A Rare Case Report
Mucopolysaccharidoses are rare hereditary lysosomal storage diseases developing due to dysfunction or deficiencies in enzymes that metabolize long-chain carbohydrates and glycosaminoglycans. Patients are normal at birth, but with accumulation of damaged products in the tissues, clinical features beg...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Galenos Yayinevi
2014-09-01
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| Series: | Haseki Tıp Bülteni |
| Subjects: | |
| Online Access: | http://www.hasekidergisi.com/article_7287/Mucopolysaccharidosis-Type-3b-In-An-Adult-With-Pancytopenia-A-Rare-Case-Report |