How do we encounter rare factor deficiencies in children? Single-centre results from Turkey

Tugcu D., Salcıoglu Z., Akçay A., Sen H. S., Aydoğan G., Akıcı F., ...Daha Fazla

BLOOD COAGULATION & FIBRINOLYSIS, cilt.26, ss.145-151, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 26
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1097/mbc.0000000000000204
  • Dergi Adı: BLOOD COAGULATION & FIBRINOLYSIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.145-151
  • Anahtar Kelimeler: childhood, clinical findings, prophylaxis, rare factor deficiency, severe bleeding, FACTOR-VII DEFICIENCY, COAGULATION DISORDERS, BLEEDING DISORDERS, PROPHYLAXIS, REGISTRY
  • İstanbul Üniversitesi Adresli: Evet

Özet

Background Rare factor deficiencies (RFDs) are autosomal recessively inherited coagulation factor deficiencies encountered at a frequency of between one in 500 000 and one in two million.