Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent

CASE REPORT

Hippokratia 2020, 24(1): 43-45

Tampaki A, Theodoridou S, Apostolou Ch, Delaki EE, Vlachaki E|

Adults Thalassemia Unit, Second Department of Internal Medicine , Haemoglobinopathy Prevention Unit, Hippokration Hospital of Thessaloniki, National Centre for Thalassemia and Hemoglobinopathies of Greece, Laiko, General Hospital of Athens, Athens, Greece

Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease

CASE REPORT

Hippokratia 2017, 21, 1: 43-45

Demosthenous C, Rizos G, Vlachaki E, Tzatzagou G, Gavra M
1st Department of Internal Medicine, Papageorgiou General Hospital, Department of Hematology and HCT Unit, George Papanicolaou General Hospital, 2nd Department of Internal Medicine, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece