A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention
TURKISH JOURNAL OF HEMATOLOGY, cilt.35, sa.1, ss.12-18, 2018 (SCI-Expanded, Scopus, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 35 Sayı: 1
- Basım Tarihi: 2018
- Doi Numarası: 10.4274/tjh.2017.0039
- Dergi Adı: TURKISH JOURNAL OF HEMATOLOGY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.12-18
- Anahtar Kelimeler: Thalassemia, Hemoglobinopathies, Splenectomy, Registries, Iron chelators, beta-thalassemia mutations, Turkey, BETA-THALASSEMIA, AEGEAN REGION, PROLONGED SURVIVAL, IRON-DEFICIENCY, HEMOGLOBIN-S, ANEMIA, POPULATION, FREQUENCY, CHILDREN, SOUTH
- İstanbul Üniversitesi Adresli: Evet
Özet
Objective: The Turkish Society of Pediatric Hematology set up a National Hemoglobinopathy Registry to demonstrate the demographic and disease characteristics of patients and assess the efficacy of a hemoglobinopathy control program (HCP) over 10 years in Turkey.