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Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases
Gaucher type 1 disease has a wide spectrum of phenotypes ranging from asymptomatic individuals to patients with massive hepatosplenomegaly and bone involvement. In most, anemia, thrombocytopenia and splenomegaly are the primary manifestations at diagnosis, findings shared by the hemoglobinopathies....
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3352325/ https://ncbi.nlm.nih.gov/pubmed/20846888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bcmd.2010.08.007 |
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