Hereditary hemorrhagic telangiectasia is characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins. Too much clotting can block blood vessels that are not bleeding consequently, the body has control mechanisms to limit clotting and dissolve clots that are no longer needed. Hereditary hemorrhagic telangiectasia is a condition characterized by abnormal blood vessels which are delicate and prone to bleeding. A child with HHT, also known as Osler-Weber-Rendu Syndrome, tends to form blood vessels that lack the capillaries between an artery and vein. It is usually referred to as the Osler-Weber-Rendu disorder, or simply the OWR. It is a rare inherited disorder that affects blood vessels throughout the body and is characterised by a tendency for bleeding in particular recurrent epistaxis, and skin telangiectasia. Hereditary haemorrhagic telangiectasia is also known as Osler-Rendu-Weber syndrome. Telangiectasias are abnormally dilated blood vessels associated with a number of diseases. In this condition, without capillaries, arterial blood under high pressure flows directly into a vein. When clotting is uncontrolled, small blood vessels in critical places can become clogged with clots. Large AVMs often cause symptoms when they occur in the brain, lungs, or gastrointestinal tract complications from bleeding or shunting may be sudden and catastrophic. Common causes and risk factor's of Hereditary Hemorrhagic Telangiectasia include the following : Some of the common sign and symptoms of the disease Hereditary Hemorrhagic Telangiectasia as follows: Find effective treatment methods of treating Hereditary Hemorrhagic Telangiectasia : Causes of Hereditary Hemorrhagic Telangiectasia
Symptoms of Hereditary Hemorrhagic Telangiectasia
Treatment of Hereditary Hemorrhagic Telangiectasia
Saturday, May 1, 2010
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