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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Medinger, Michael, Saller, Elisabeth, Harteveld, Cornelis L, Lehmann, Thomas, Graf, Lukas, Rovo, Alicia, Buser, Andreas, Passweg, Jakob, Tichelli, André
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: PAGEPress Publications 2011
Aiheet:
Case Report
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia