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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Hlavní autoři:	Michael Medinger, Elisabeth Saller, Cornelis L. Harteveld, Thomas Lehmann, Lukas Graf, Alicia Rovo, Andreas Buser, Jakob Passweg, André Tichelli
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	MDPI AG 2011-12-01
Edice:	Hematology Reports
Témata:	alpha-Thalassemia HbH disease iron deficiency sickle cell trait
On-line přístup:	http://www.pagepress.org/journals/index.php/hr/article/view/3524
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