Conn's syndrome

Conn's syndrome, also known as primary hyperaldosteronism, is a health condition characterized by the overproduction of the hormone aldosterone by the adrenal glands, which are located above the kidneys. Aldosterone plays a crucial role in regulating blood pressure by controlling the balance of sodium and potassium in the body. When too much aldosterone is produced, it causes the kidneys to retain sodium and lose potassium, leading to increased water retention, high blood pressure (hypertension), and low potassium levels (hypokalemia). Common symptoms of Conn's syndrome include persistent high blood pressure that is difficult to control, muscle weakness, fatigue, headaches, excessive thirst, and frequent urination. In some cases, patients may also experience tingling or numbness due to the low potassium levels. Diagnosis typically involves blood tests to measure aldosterone and renin levels, as well as imaging studies like CT scans to identify any abnormalities in the adrenal glands. Treatment options for Conn's syndrome may include medications that block the effects of aldosterone, lifestyle changes such as a low-sodium diet, or surgical removal of the affected adrenal gland if a benign tumor (adenoma) is present. Early detection and management of Conn's syndrome are crucial, as untreated high blood pressure can lead to serious complications, including heart disease, stroke, and kidney damage. Understanding Conn's syndrome and its impact on health can help individuals seek appropriate medical care and improve their overall well-being.