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Fanconi Anemia with Incidental Haemoglobin E Trait: The First Reported Case in Literature
Fanconi anemia (FA), commonly inherited as an autosomal recessive trait, is the commonest cause of inherited bone marrow failure syndrome often accompanied by skeletal deformities, genitourinary abnormalities and an increased risk of malignancies especially acute myeloid leukemia. Haemoglobin E ((β2...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer India
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4192169/ https://ncbi.nlm.nih.gov/pubmed/25332553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-013-0279-7 |
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