Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case PresentationA. Agapidou1, S. Theodoridou1, K. Tegos3, E. Mandala4, E. Leukou1, O. Karakasidou1, B. Aletra1, A. Sevastidou1, M. Alemayehou1, E. Voskaridou2 1Hippokration Hospital Of Thessaloniki, Hemoglobinopathy Prevention Unit, Thessaloniki, Greece 2Laikon Hospital Of Athens, Thalassemia Center, Athens, Greece 3Nımıts, Military Hospital, Athens, Greece 4Aristotelion University Of Thessaloniki, 4th Unit Of Internal Medicine, Thessaloniki, Greece Keywords: -
Kalıtsal Pirimidin 5’- Nükleotidaz Eksikliği ve Alfa Talasemi Taşıyıcı Birlikteliği: Olgu SunumuA. Agapidou1, S. Theodoridou1, K. Tegos3, E. Mandala4, E. Leukou1, O. Karakasidou1, B. Aletra1, A. Sevastidou1, M. Alemayehou1, E. Voskaridou2 1Selanik Hippokration Hastanesi Hemoglobinopati Önleme Birimi, Selanik, Yunanistan 2Atina Laikon Hastanesi, Talasemi Merkezi, Atina, Yunanistan 3Nımıts, Asker Hastanesi, Atina, Yunanistan 4Selanik Aristotelion Üniversitesi, İç Hastalıkları 4. Ünitesi, Selanik, Yunanistan Anahtar Kelimeler: -
A. Agapidou, S. Theodoridou, K. Tegos, E. Mandala, E. Leukou, O. Karakasidou, B. Aletra, A. Sevastidou, M. Alemayehou, E. Voskaridou. Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation. Turk J Hematol. 2012; 29(4): 433-435
Corresponding Author: A. Agapidou, Greece |
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