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Hereditary Thrombophilia

Background

Hereditary Thrombophilia is the increased tendency to develop blood clots in veins and arteries. Blood is designed to flow freely round the body and not obstruct blood vessels. At the time of a cut, however, blood thickens and becomes sticky around the injured area forming a semi-solid mass (otherwise known as a blood clot or thrombus). This prevents bleeding and limits blood loss. In thrombophilia, clotting most often occurs within an unbroken vessel at an inappropriate time and place.

Blood clots may form within all blood vessels, but typically occur in the large vessels in the brain, heart, lungs, legs and arms. Clots in the leg or the arm can usually be detected by ultra-sound examination. In addition, clots can be detected by X-ray examination by injecting a substance into the blood to make the clot stand out. A blood clot in the lung is more difficult to diagnose. A radioactive substance may be used to test for a mismatch between the distribution pattern of blood flowing in the vessels and of the air filled spaces in the lungs. Such a mismatch would indicate the presence of a clot.

What are the symptoms? View What are the symptoms?

Medical text written February 2002 by Contact a Family. Approved February 2002 by Professor F Cotter, Professor of Experimental Haematology, St Bartholomew's Hospital, London, UK.

 

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