Case Study of a Rare Genetic Disorder: Gaucher Disease
Gaucher disease (GD) is a rare, autosomal recessive genetic disorder characterized by the accumulation of fat-laden Gaucher cells in organs such as the spleen, liver, and bone marrow. The condition presents with a range of symptoms, including hepatosplenomegaly, anemia, thrombocytopenia, fatigue, an...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
International Medical Research and Development Corporation
2025-06-01
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| Series: | International Journal of Biomedicine |
| Subjects: | |
| Online Access: | http://www.ijbm.org/articles/i58/ijbm_15(2)_cr1.pdf |
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