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Treatment Of Recalcitrant Chronic Leg Ulcer In A Known Sickle Cell Anaemia Patient Using Honey and Fresh HbAA Red Cell Concentrate In A Nigerian Secondary Healthcare Facility
Sickle hemoglobin (HbS) formed by the point mutation in the genetic code of beta-globin chain leading to valine substituting glutamic acid at position 6 of the beta-chain. The resultant sickle cell disease (SCD) characterized by occlusion of microvasculature by red blood cells is associated with mul...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015949/ https://www.ncbi.nlm.nih.gov/pubmed/33243953 http://dx.doi.org/10.4103/aam.aam_53_19 |