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Can people with CAH have children? The most common is 21- hydroxylase deficiency, which makes up about 95 percent of cases. A child with this type of CAH has adrenal glands that cannot make enough cortisol and may or may not make aldosterone. Children with this type of CAH may have high blood pressure. These patients do not have aldosterone deficiency.
How is congenital adrenal hyperplasia diagnosed? Diagnosis of CAH includes: Physical exam. The doctor examines your child and evaluates symptoms. Blood and urine tests. Tests used to diagnose CAH measure levels of hormones produced by the adrenal glands. Gene testing. Testing to determine a child's sex.
What are the side effects of having your adrenal gland removed? Symptoms can include headache, sweating, palpitations (rapid heart beats), and high blood pressure. There will also be high levels of catecholamines (epinephrine and norepinephrine) in the urine and blood. Most adrenal tumors can be removed by a surgical procedure called laparoscopic adrenalectomy.
What does congenital adrenal hyperplasia do? Congenital adrenal hyperplasia is an inherited condition caused by mutations in genes that code for enzymes involved in making steroid hormones in the adrenal glands. The most common enzyme defect, 21-hydroxylase deficiency, leads to excess amounts of male hormones being produced by the adrenal glands.
Is congenital adrenal hyperplasia curable? Although there is no cure, with proper treatment, most people with congenital adrenal hyperplasia can lead normal lives.
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