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An “acquired” hemoglobin J variant in a sickle cell disease patient

We report the case of a rare hemoglobin variant, “Hemoglobin J”, discovered while performing hemoglobin electrophoresis following exchange transfusion of a sickle cell disease patient. It is usual practice in our institution to confirm the hemoglobin S level in sickle cell disease patients after red...

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Detalles Bibliográficos
Autores principales: Swedan, Nawwar, Nicol, Kathleen, Moder, Phylis, Kahwash, Samir
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2500260/
https://www.ncbi.nlm.nih.gov/pubmed/18827863