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Treatment Details

Congenital Adrenal Hyperplasia (CAH)

Overview

Congenital adrenal hyperplasia (CAH) is a collection of genetic disorders that impact the adrenal glands, which are responsible for producing essential hormones for bodily functions. Any disruption in these hormones can lead to symptoms that influence sexual development. The treatment involves administering different steroids to compensate for the hormones that the body is unable to produce.

Symptoms of Congenital Adrenal Hyperplasia (CAH)

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Diagnosis of Congenital Adrenal Hyperplasia (CAH)

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Causes of Congenital Adrenal Hyperplasia (CAH)

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Treatment Options / Stages of Congenital Adrenal Hyperplasia (CAH)

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Frequently Asked Questions

Q: Is There a Cure for Congenital Adrenal Hyperplasia?
A: Though it cannot be cured, CAH can be successfully managed. The patient must receive treatment for classical CAH from the time of birth till the end of their life.

Q: What Is the Most Effective CAH Treatment?
A: Adults receive dexamethasone, prednisone, or hydrocortisone in place of cortisol. Fludrocortisone is an additional medication taken by patients with classic CAH in place of aldosterone. Salt-wasters may also be able to retain salt by consuming salty foods or taking salt supplements.

Q: Can Someone with CAH Lead a Regular Life?
A: You must understand that CAH is a medical disorder that can be fully treated. The youngster with CAH can lead an entirely normal life, save from the requirement to take medication on a daily basis.

Q: What Hormone Is Responsible for CAH?
A: In congenital adrenal hyperplasia (CAH), a mutation (genetic alteration) causes the adrenal glands to produce insufficient cortisol.

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Treating doctor asks for detailed history of the patients, chronology of investigations done, treatments undertaken, current symptoms to arrive at the right line of treatment and share the expected cost of treatment.