What is Osler Weber Renda?

Ossler Weber Renda is a genetic disorder characterized by irregular blood vessels throughout the body. The condition results in a skin lesion and severe internal or external bleeding. Ossler Weber Rendu syndrome requires lifelong driving.

also known as hereditary hemorrhagic telangiectasia, occurs when capillaries do not normally develop. As a result, veins and arteries are directly connected in certain areas of the body. Veins and arteries have different pressure levels, so the rupture tends to occur in places where both systems meet.

People who have this condition often have purple red clusters of blood vessels called thinangiectas on the face, lips, tongue and fingers, as well as other areas of the body. These clusters break and bleed easily. Some patients also suffer from frequent and heavy noses.

Many of these patients experience bleeding inside and out. They could have a black or tar stool, indicating bleeding into the gastrointestinal tract or could inykašat blood. Some people experience serious complications such as high blood pressure, stroke or heart failure from bleeding inside the brain or body.

Ossler Weber Rendu syndrome is most commonly seen in people of Caucasian origin, but it can also affect people of Asian, African and Arab origin. The disorder affects the same man and woman. Usually occurs at the age of 30.

Doctor who suspects that Zelera Weber Renda syndrome has performed a complete physical examination. He will look at his face and body at the presence of telangiectas and perform blood tests to check the anemia. Blood ability is also measured normally.

The doctor can also perform X-rays of the chest to look for arterio-life malformations (AVM) on the lungs or order magnetic resonance imaging (MRI) for a look for brain bleeding. If bleeding occurs in the gastrointestinal tract, the doctor may perform endoscopy. In thisThe test is selected by a long flexible tube equipped with a small camera photo from the inside of the body.

Doctors treat Osler Weber Renda syndrome based on the patient's needs. Some people suffering from frequent noses benefit from estrogen therapy. Others may require surgical cautery to treat areas that bleed often. Some patients require blood transfusions from time to time, depending on the severity of the condition.

OSLER Weber Syndrome does not affect the patient's mental or cognitive abilities and usually does not reduce the patient's life. Parents can hand over the failure to their children. A genetic advisor can advise a future parent who has the history of illness in his family.