- ... people with this disorder have few if any symptoms. The most common feature of factor XI deficiency is prolonged bleeding after trauma or surgery, especially ...
- ... Hemophilia B XL Clinically indistinguishable from hemophilia A Diagnosis is based on factor IX clotting activity <40%. F11 Factor XI deficiency (OMIM 612416 ) AR AD Compound heterozygous & homozygous persons ...
- ... have activity <1%-15%. 1 A specific factor XI clotting assay establishes the diagnosis. F12 KLKB1 KNG1 Factor XII (OMIM 234000 ), prekallikrein (OMIM 612423 ), or high molecular-weight kininogen deficiencies (OMIM 228960 ) AR Not assoc w/clinical bleeding ...
- ... copy of the mutated gene and have partial factor XI deficiency; they rarely show severe signs and symptoms of the condition.In some families, this condition ...
- ... usually do not experience abnormal bleeding or other symptoms. Factor XII deficiency is typically discovered during routine blood testing because ...
- ... COL11A1 gene are among many genetic and environmental factors that likely influence this complex disease. COBA1_HUMAN COLL6 collagen type XI alpha 1 collagen XI, alpha-1 polypeptide collagen, ...
- ... in women with von Willebrand's disease or factor XI deficiency. Br J Obstet Gynaecol. 1998 Mar; 105 :314– ... labor is not mandatory for women with severe factor XI deficiency. Blood Coagul Fibrinolysis. 2005 Jan; 16 :37–41. ...
- ... topic><topic ><url >https://medlineplus.gov/genetics/condition/factor-xi-deficiency</url><title >Factor XI deficiency</title><other_names ><other_name >F11 deficiency</other_ ...
- ... 2015] ~100% 3 1/21 Iranian Jewish F11 Factor XI deficiency (OMIM 612416 ) AR c.403G>T p.Glu135Ter ( ... O, Seligsohn U. The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ...
- ... V deficiency Factor VII deficiency Factor X deficiency Factor XI deficiency (hemophilia C) Glanzmann disease Hemophilia A Hemophilia B Idiopathic thrombocytopenic purpura (ITP) Von Willebrand disease (types I, II, and III)
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