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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