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A Rare Case of Hemoglobin E Hemoglobinopathy with Gaucher’s Disease
Hemoglobin (Hb) E mutation is common in north-east part of our country. The natural history of Hb E thalassemia is highly variable. The phenotype, for patients with similar mutations, can range from asymptomatic to transfusion dependent. Our patient presented at 2 years of age with failure to thrive...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer-Verlag
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3636348/ https://ncbi.nlm.nih.gov/pubmed/24426351 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-012-0153-z |
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