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


Tugcu D., Salcioglu Z., Akcay A. , Sen H. S. , Aydogan G., Akici F., et al.

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

  • Cilt numarası: 26 Konu: 2
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1097/mbc.0000000000000204
  • Dergi Adı: BLOOD COAGULATION & FIBRINOLYSIS
  • Sayfa Sayısı: ss.145-151

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.