Conn's Syndrome

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Understanding Conn’s Syndrome (Primary Hyperaldosteronism)

What is Conn’s Syndrome?

Conn’s Syndrome, also known as primary hyperaldosteronism, is a condition characterized by the overproduction of aldosterone, a hormone produced by the adrenal glands. Aldosterone helps regulate blood pressure by controlling sodium and potassium levels in the body. In Conn’s Syndrome, excessive aldosterone causes the body to retain sodium and lose potassium, leading to high blood pressure (hypertension) and low potassium levels (hypokalemia). Early diagnosis and treatment are essential to prevent complications such as heart and kidney damage.

Symptoms of Conn’s Syndrome

Common symptoms of Conn’s Syndrome include high blood pressure that is resistant to standard treatments, fatigue, muscle weakness, excessive thirst, frequent urination, and headaches. Severe potassium deficiency may lead to muscle cramps, palpitations, or even paralysis in rare cases. Some individuals may not exhibit noticeable symptoms, with the condition only detected during evaluations for persistent hypertension.

Consult with Dr. Zaar

If you're struggling with this condition, consult with Dr. Zaar, a specialist in diagnosing and treating disorders like yours. With expertise in advanced medical treatments and personalized care plans, Dr. Zaar is committed to addressing your unique needs and improving your quality of life. Take the first step towards better health

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FAQs

1. What causes Conn’s Syndrome?
Conn’s Syndrome is primarily caused by a benign tumor (aldosterone-producing adenoma) on one adrenal gland or bilateral adrenal hyperplasia (overgrowth of both glands).

2. How is Conn’s Syndrome diagnosed?
Diagnosis involves blood tests to measure aldosterone and renin levels, imaging tests (CT or MRI) to detect adrenal abnormalities, and confirmatory tests like a saline infusion test.

3. Is Conn’s Syndrome hereditary?
While most cases are not hereditary, certain forms, such as familial hyperaldosteronism, may have a genetic component.

4. How is Conn’s Syndrome treated?
Treatment depends on the cause. Surgical removal of the affected adrenal gland (adrenalectomy) is often recommended for aldosterone-producing adenomas, while aldosterone-blocking medications (e.g., spironolactone or eplerenone) are used for bilateral adrenal hyperplasia.

5. Can Conn’s Syndrome be cured?
In many cases, surgical removal of the affected adrenal gland can cure the condition. Medication can effectively manage symptoms in other cases.

6. What are the risks of untreated Conn’s Syndrome?
Untreated Conn’s Syndrome can lead to complications such as heart disease, kidney damage, stroke, and persistent hypertension.

7. How common is Conn’s Syndrome?
Conn’s Syndrome is relatively rare but is increasingly recognized as a cause of secondary hypertension, affecting about 5-10% of individuals with high blood pressure.

8. Can diet help manage Conn’s Syndrome?
A low-sodium diet can help reduce blood pressure and alleviate some symptoms, especially when combined with medical treatments.

9. Can Conn’s Syndrome occur in both men and women?
Yes, Conn’s Syndrome affects both genders, though it is slightly more common in women, especially between the ages of 30 and 50.

10. When should I see a doctor for Conn’s Syndrome?
Seek medical attention if you have high blood pressure that is difficult to control, persistent muscle weakness, or other symptoms like excessive thirst and frequent urination.