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Aldosterone level test
Aldosterone level test


Congenital adrenal hyperplasia

Alternative Names:
Adrenogenital syndrome; 21-hydroxylase deficiency

Treatment:

The goal of treatment is to return hormone levels to normal. This is achieved by daily administration of forms of cortisol: dexamethasone, fludrocortisone, or hydrocortisone. Additional doses of medicine are required during times of stress such as severe illness or surgery.

Text Continues Below



The gender of a baby with ambiguous genitalia is determined by examination of the chromosomes (karyotyping). Reconstructive surgery for girls with masculine external genitalia is usually performed between the ages of 1 and 3 months to correct the abnormal appearance.

Parents of children with this disorder need instruction on the side effects of steroid therapy. They should report signs of infection and stress to their health care provider because increases in medication may be required. In addition, steroid medications cannot be stopped suddenly or adrenal insufficiency will result.



Support Groups:

National Adrenal Diseases Foundation: (516) 487-4992

CARES (Congenital Adrenal hyperplasia Research, Education, and Support) Foundation: (866) 227-3737 (toll free) or www.caresfoundation.com



Expectations (prognosis):

The outcome is usually associated with good health, but short stature may result even with treatment. Males have normal fertility. Females may have a smaller opening of the vagina and lower fertility.

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