Ovrena Disease

Ovren's disease is a disease from the category of cancerous tumors of hereditary nature. It first became known at the end of the 19th century. Hematologists all over the world treat this problem. Experts have given this unpleasant “neighborhood” poetic “nicknames”: hematokeratoma and osteosarcoma. There are several theories about the origin of the disease. Experts believe that this pathological process is nothing more than a mutation of endothelial cells. They multiply and spread throughout the body. A person loses blood with secretions of red blood cells as their outer shell. There is a thickening of the bloodstream and destruction of many tissue cells. As a result, open wounds appear. That is why another name appeared for this disease - hemofibrosis. The progression of the disease is characterized by a strong manifestation of vascular pathology. Often the formation of sclerotic growths begins in the lower extremities, then gradually spreads to other parts of the body. The neoplasm is complicated by the inability to eat normally and heal quickly. This disease most often affects the fair sex. In addition, there is a hereditary predisposition to the appearance of seals. The disease also occurs in pregnant women, smokers and patients with hypertension. Gradually, the villi are destroyed, and after they die, the growth of a cancerous tumor begins. Metastases penetrate the bone marrow and destroy the blood. Blood clots form in the affected areas. The skin becomes loose and hot to the touch. Patients feel throbbing pain in the legs, venous nodes. The bones fuse together and the foot becomes deformed, resulting in a loss of the ability to move independently without the help of others. Bone tissue changes color and becomes pink. Doctors say surgery is the only way to slow the progression of the disease. However, for many people this is simply impossible due to the large spread of the tumor throughout the body. Prevention methods can reduce the risk of developing the disease. This is following a diet with a limitation of strong tea, coffee, alcoholic beverages and the consumption of large volumes of liquid. You can't get too cold. Even a short stay in cool water is equivalent to frostbite. Preference should be given to clothing made from natural fibers. It helps to pass air faster, absorbs moisture well and is hygroscopic. Regular walking strengthens your leg muscles. Doctors recommend hardening. The advanced stage of the disease is an indication for surgical treatment. After surgery, you should be under medical supervision and

Currently, there are many incurable diseases for which treatment is therapy. One of these diseases is ovrenia disease. This is a genetic disease that manifests itself as disorders in the blood system. Ovren's disease is characterized by dysfunction of erythropoiesis, the process responsible for the formation of red blood cells in the bone marrow. In simple words, this disease leads to a decrease in the level of hemoglobin in the blood, which causes weakness and other disorders. This is a rare disease that was first discovered in 2010. It is inherited and can occur in both sexes. Most often, the disease is detected in people living in northern Norway. Ovren's disease is inherited as a recessive trait, so the risk of transmitting the disease to children is 25%.

The main cause of the disease is a mutation in the OCA2 gene, which plays an important role in the proper production of the key protein subunit of hemoglobin, which is responsible for the transfer of oxygen to red blood cells. The main symptom of the disease is a significant decrease in hemoglobin levels and anemia. Complications such as ischemic stroke, thrombosis and others are possible. However, this is not the only sign of the disease, and each patient, depending on the severity of the situation, may be susceptible to different manifestations of the disease. For example, you may experience: - dizziness; - chest pain; - muscle weakness; - headache; - pallor; - cold extremities; - shortness of breath. Treatment for ovarian disease is very complex and involves a combination of several methods: blood transfusions and medications to reduce the likelihood of blood clots, as well as bone marrow transplantation. In addition, patients regularly require blood transfusions to maintain hemoglobin levels. It's important to note that symptoms of Ovren may not appear until middle age, so it's important to monitor your family's health and get regular medical checkups.

Ovren's disease is a hereditary disorder of hemostasis characterized by an inadequate increase in the level of natural fibrinolysis inhibitors and factor Xa inhibitor. This defect causes fibrin arrest at the vWF level and excess fibrin after skin incision or endothelial injury. It is transmitted by autosomes