A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency

We present a case of a 40-year-old female from Turkey, who was referred to our outpatient clinic for an undetermined thalassemia and sickle cell trait. At first consultation hemoglobin was decreased (71 g/L) with microcytosis (MCV 55.1 fL), and hypochromia (MCHC 239 g/L). The patient had severe iron...

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Detalhes bibliográficos
Main Authors: Medinger, Michael, Saller, Elisabeth, Harteveld, Cornelis L, Lehmann, Thomas, Graf, Lukas, Rovo, Alicia, Buser, Andreas, Passweg, Jakob, Tichelli, André
Formato: Artigo
Idioma:Inglês
Publicado em: PAGEPress Publications 2011
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3269802/
https://ncbi.nlm.nih.gov/pubmed/22593821
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/hr.2011.e30
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