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This template may be used to display a person's or entity's whole lifespan in years, and optionally their final age or duration, also in years; the Gregorian calendar and AD/CE era are respectively, the implied default calendar and editable default era. Astronomical dates are not specifically handled; negative years are not allowed, but year '0' (zero) may be used when applicable. All date ...
This template may be used to display a person's or entity's whole lifespan in years, and optionally their final age or duration, also in years; the Gregorian calendar and AD/CE era are respectively, the implied default calendar and editable default era. Astronomical dates are not specifically handled; year '0' (zero) cannot be rendered. For details and examples see the template's documentation ...
Haemophilia (British English), or hemophilia (American English) [6] (from Ancient Greek αἷμα (haîma) 'blood' and φιλία (philía) 'love of'), [7] is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.
Joint capsule. Haemophilia A's phenotype has a quite wide range of symptoms encompassing both internal and external bleeding episodes. Individuals with more severe haemophilia tend to experience more intense and frequent bleeding, whereas those with mild haemophilia typically exhibit milder symptoms unless subjected to surgical procedures or significant trauma.
X chromosome. The factor IX gene is located on the X chromosome (Xq27.1-q27.2). It is an X-linked recessive trait, which explains why males are affected in greater numbers. [9] [10] A change in the F9 gene, which makes blood clotting factor IX (9), causes haemophilia B. [11]
Acquired haemophilia A (AHA) is a rare but potentially life-threatening bleeding disorder characterized by autoantibodies directed against coagulation factor VIII.These autoantibodies constitute the most common spontaneous inhibitor to any coagulation factor and may induce spontaneous bleeding in patients with no previous history of a bleeding disorder.
The World Federation of Hemophilia (WFH) is an international non-profit organization dedicated to improving the lives of people with hemophilia (also spelled haemophilia) and other genetic bleeding disorders. It educates people with bleeding disorders and lobbies for improved medical treatment.
The National Bleeding Disorders Foundation was founded in 1948, as the first national hemophilia advocacy organization in the United States. [2] One of its early initiatives was to secure funding for Comprehensive Hemophilia Diagnostic and Treatment Centers (HTC).