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

Tugcu, DENİZ; Salcıoglu, Zafer; Akçay, Arzu; Sen, Hulya; Aydoğan, Gonul; Akıcı, Ferhan; Keskindemirci, GONCA; Ayaz, NURAY; Baslar, Zafer

doi:10.1097/mbc.0000000000000204

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, Scopus)

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.