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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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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer India
2013
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| 主題: | |
| オンライン･アクセス: | 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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