How do we encounter rare factor deficiencies in children? Single-centre results from Turkey
BLOOD COAGULATION & FIBRINOLYSIS, vol.26, pp.145-151, 2015 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 26
- Publication Date: 2015
- Doi Number: 10.1097/mbc.0000000000000204
- Journal Name: BLOOD COAGULATION & FIBRINOLYSIS
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.145-151
- Keywords: childhood, clinical findings, prophylaxis, rare factor deficiency, severe bleeding, FACTOR-VII DEFICIENCY, COAGULATION DISORDERS, BLEEDING DISORDERS, PROPHYLAXIS, REGISTRY
- Istanbul University Affiliated: Yes
Abstract
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.