Bernheim Syndrome

p. bernhelm - Borg-Wilson syndrome

In a pathological heart condition called Borg-Wilenskirche syndrome, for as yet unknown reasons, blood pressure increases in the atria. It puts pressure on the valve flaps, the pores of which are narrowed due to illness. They become ineffective as a result of continued exposure to blood, this leads to disruption, as well as structural destruction of the valvular apparatus of the heart. With such damage, the contractility of the heart can significantly deteriorate, increasing the risk of thromboembolic events and sudden death. Already with a single presence of high pressure

Good day to everyone who reads this article! In this article we will talk about Bernheim syndrome - this is a fairly rare genetic disease that is characterized by abnormalities in the human genome system.

**What kind of syndrome is this?** This disease is congenital and appears when a child has reduced protein activity (protein is an important component of the structure of chromosomes). Due to a decrease in the activity of this protein, the formation of chromosomes is disrupted, which leads to their abnormal development and the appearance of anomalies. This disease is also known as Rausenne Syndrome.

Anomalies in Bernheim syndrome can be very diverse. Scientists still don’t know exactly why such disorders occur. But there are several hypotheses about the cause of the syndrome: - Genetic factors that lead to a decrease in protein activity; - External environment (quality of nutrition, environment, maternal health); - Viruses, bacteria or infections that are transmitted to the child from the mother through the placenta during pregnancy - they may cause the development of the syndrome in the fetus;

The most common external signs of Bernheim syndrome: * deformation of the limbs; * developmental delay; * lack of teeth;

What to do if you are diagnosed with Bernheim syndrome? If you have been diagnosed with this disease, then first of all you and your loved ones need to calm down. After all, the key to successful treatment is **psychological support**. Currently, treatment for this syndrome consists of selecting some specialized medications in order to improve the functioning of cells. Therapeutic measures are also used to improve the patient’s quality of life; in addition, a person who suffers from this syndrome should conduct consultations with specialists - pediatricians, cardiologists and other specialists, since timely prescribed treatment has a positive effect. All face-to-face treatment measures are individual and depend on the characteristics of the patient’s body. But you should always remember that if you did not manage to recognize this disease in time and prescribe treatment, in children with it the pathology can lead to dysfunction of the heart.