A Rare Case of Compound Heterozygous Sickle Cell Beta Thalassaemia with High HbF and Normal HbA2 Levels Detected on HPLC
Compound heterozygous Sickle Haemoglobin (HbS) beta (β) thalassaemia arises from the mutations associated with sickle cell and β thalassaemia and significantly affects populations in low income countries like India. Elevated levels of Haemoglobin A2 (HbA2) represent the primary indicator for identif...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
JCDR Research and Publications Private Limited
2024-05-01
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| سلاسل: | Journal of Clinical and Diagnostic Research |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://jcdr.net/articles/PDF/19436/69437_CE[Ra1]_F(IS)_PF1(KB_DK_OM)_redo_Ref_Pat(OM)_PFA(SS)_PB(KB_OM)_PN(OM).pdf |
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