Haemophilia b D67

Author: Prof. Dr. med. Peter Altmeyer

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Last updated on: 29.10.2020

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Synonym(s)

Christmas disease; Factor IX deficiency; Factor IX Deficiency; HEMB; Hemophilia; Hemophilia B

History
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Aggeler et al, 1952; Biggs et al, 1952

Definition
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Hereditary activity deficiency of factor IX (Christmas factor) with reduced blood thromboplastin formation, reduced conversion of prothrombin to thrombin and reduced conversion of fibrinogen to fibrin.

Occurrence/Epidemiology
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Proportion of all haemophilia diseases: 20-25%. Incidence (Federal Republic of Germany): 1/20,000 men.

Etiopathogenesis
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X-linked mutations of the HEMB coagulation factor IX gene (HEMB gene; F9 gene; gene locus: Xq27.1-q27.2 F9).

Manifestation
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Mostly occurring in men. Women are conductors.

Clinical features
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Small area bleeding after minor trauma. Characteristic recurrent bleeding in muscles and joints with subsequent muscular atrophies and contractures, joint stiffening. More frequent spontaneous haemorrhaging in severe haemophilia in adolescence (great urge to move), rare in moderately severe haemophilia.

Laboratory
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  • Severe haemophilia: factor IX < 1%. Medium haemophilia: factor IX 1-4%.
  • Mild haemophilia: factor IX 5-25%.
  • Subhemophilic hemophilia: factor IX 25-45%. Bleeding time: normal; clotting time: prolonged; quickset: normal; prothrombin consumption: reduced.

Internal therapy
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Substitution of factor IX.

Literature
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  1. Aggeler PM, White SG, Glendening MB, Page EW, Leake TB, Bates G (1952) Plasma thromboplastin component (PTC) deficiency: a new disease resembling hemophilia. Proc Soc Exp Biol Med 79: 692-694
  2. Biggs R, Douglas AS, Macfarlane RG, Dacie JV, Pitney WR, Merskey C, O'Brien JR (1952) Christmas disease: a condition previously mistaken for haemophilia. Brit Med J 2: 1378-1382

Incoming links (1)

Haemophilia;

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Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

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Last updated on: 29.10.2020