A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention


Aydinok Y., Oymak Y., Atabay B., Aydogan G., Yesilipek A., Unal S., ...Daha Fazla

TURKISH JOURNAL OF HEMATOLOGY, cilt.35, sa.1, ss.12-18, 2018 (SCI-Expanded) identifier identifier identifier

  • 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.