What is bartter sendromu?

Bartter syndrome is a rare genetic disorder that affects how the kidneys function. It is caused by mutations in genes that are responsible for regulating salt and fluid balance in the body. As a result, people with Bartter syndrome experience a variety of symptoms, including excessive urination, dehydration, low blood pressure, muscle weakness, and fatigue.

There are several types of Bartter syndrome that vary in terms of severity and age of onset. Some people with the syndrome may only experience mild symptoms that do not significantly impact their daily lives, while others may require ongoing medical care to manage more severe symptoms.

Treatment for Bartter syndrome typically involves addressing specific symptoms as they arise. This may include taking medications to help regulate fluid and electrolyte levels in the body, as well as making dietary changes to maintain a healthy balance of nutrients. In severe cases, some people with Bartter syndrome may require dialysis or kidney transplantation to manage their symptoms.