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Congenital adrenal hyperplasia

Congenital adrenal hyperplasia is the name given to a group of inherited disorders of the adrenal gland. Inherited means the traits are passed down from parent to child.


Your adrenal glands are 2 walnut-sized organs that sit one on top of each kidney. The adrenal glands make the following hormones that are essential for life.

  • Cortisol regulates blood pressure, blood sugar, and energy levels. It also helps your body respond to illness and stress.
  • Aldosterone helps manage sodium and potassium levels in your blood to help regulate blood pressure.
  • Androgens are male sex hormones, such as testosterone. These hormones play a role in growth and development in both males and females.

Most people with congenital adrenal hyperplasia (CAH) lack an enzyme called 21-hydroxylase. The adrenal glands need this enzyme to make enough cortisol and aldosterone. Because of low cortisol levels, the body stimulates the adrenal gland, which then produces more androgen. This results in an imbalance of these hormones.

There are two main types of CAH that make up most of all cases: classic CAH and nonclassic CAH.

Classic CAH is rarer and more serious. It is often found at birth or early infancy. The body makes too little aldosterone and cortisol and too much androgen. There are two subtypes of classic CAH:

  • Salt-wasting CAH. This is the most serious form, and it can cause life-threatening symptoms. The body makes too little aldosterone to regulate the sodium levels in the blood. This results in loss of sodium through the urine. It can be life-threatening without treatment.
  • Simple-virilizing CAH. This more moderate form of CAH does not cause life-threatening symptoms. The body makes enough aldosterone to regulate sodium levels, but it still produces too little cortisol and too much androgen.

Nonclassic CAH is the mildest and most common form. The body produces enough aldosterone and cortisol, but too much androgen. It often is not diagnosed until later in childhood or adulthood. The person may not have any or only mild symptoms.


Symptoms will vary, depending on the type of CAH someone has and their age when the disorder is diagnosed.

  • Females with classic CAH often have ambiguous genitalia at birth and may be diagnosed before symptoms appear.
  • Males have typical male genitalia at birth, even if they have a more severe form.

In children classic, salt-wasting CAH, several adrenal symptoms often develop within 2 or 3 weeks after birth. They may include:

  • Poor feeding or vomiting
  • Diarrhea
  • Dehydration
  • Electrolyte changes (abnormal levels of sodium and potassium in the blood)
  • Abnormal heart rhythm
  • Low blood glucose
  • Too much acid in the blood (metabolic acidosis)
  • Weight loss
  • Shock

Females with nonclassic CAH will usually have normal female reproductive organs (ovaries, uterus, and fallopian tubes). They may also have the following changes:

  • Abnormal menstrual periods or failure to menstruate
  • Early appearance of pubic or armpit hair
  • Severe acne
  • Excessive hair growth or facial hair
  • Some enlargement of the clitoris

Males with nonclassic CAH often appear normal at birth. However, they may appear to enter puberty early. Symptoms may include:

  • Deepening voice
  • Severe acne
  • Early appearance of pubic or armpit hair
  • Enlarged penis but normal testes
  • Well-developed muscles

Both males and females will grow rapidly during childhood, but be much shorter than normal as adults.

Exams and Tests

If you have a family history of CAH, you may want to talk with your health care provider about having prenatal tests to check for the disorder in your unborn baby:

At birth, your child will be screened for CAH as part of newborn screening tests. This is done with a heel stick to draw blood (as part of the routine screenings done on newborns). However, this can only detect classic CAH.

If a person has symptoms of any type of CAH, the provider will do an exam and order certain tests. Common blood tests include:

Genetic tests can help diagnose or confirm the disorder, but they are rarely needed.


The goal of treatment is to return hormone levels to normal, or near normal. Treatment may include taking:

  • Hydrocortisone to replace cortisol
  • Fludrocortisone to replace aldosterone
  • Salt supplements

Medicine should be taken daily. People may need additional doses of medicine during times of stress, such as severe illness or surgery. Lifelong monitoring is needed to ensure that proper hormone levels are maintained.

Steroids (such as hydrocortisone and fludrocortisone) used to treat CAH do not usually cause side effects such as obesity or weak bones, because the doses replace the hormones that the body cannot make. Steroids cannot be stopped suddenly because doing so may lead to adrenal crisis.

People with nonclassic CAH may not need medicine or just need low doses of medicine.

A team of health care professionals with expertise in CAH will work together to treat the child and support the family. This team may include neonatologists, geneticists, endocrinologists, and psychiatrists or social workers.

Female children with ambiguous genitalia may need surgery to improve function and to create a more typical female appearance. Many health experts suggest waiting until the child is old enough to be involved in the decision, unless surgery is needed for the health of the infant. Talk with your child’s health care providers about what may be best for your child.

Working with a mental health professional is an important part of a treatment plan for children with CAH and their families.

Support Groups

More information and support for people with CAH and their families can be found at:

Outlook (Prognosis)

Most people with this disorder must take medicine their entire life. They most often have good health. However, they may be shorter than normal adults, even with treatment.

In some cases, CAH can affect fertility.

Possible Complications

Adrenal crisis is a serious complication of classic CAH.


Because this is a genetic condition, there is no way to prevent it. However, parents with a family history of CAH (of any type) or a child who has the condition should consider genetic counseling.

Alternative Names

Adrenogenital syndrome; 21-hydroxylase deficiency; CAH


Donohoue PA. Disorders of sex development. In: Kliegman RM, St Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics. 21st ed. Philadelphia, PA: Elsevier; 2020:chap 606.

Escobar O, Gurtunca N, Viswanathan P, Witchel SF. Pediatric endocrinology. In: Zitelli BJ, McIntire SC, Nowalk AJ, Garrison J, eds. Zitelli and Davis' Atlas of Pediatric Physical Diagnosis. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 9.

Eunice Kennedy Shriver National Institute of Child Health and Human Development website. Congenital adrenal hyperplasia (CAH). Updated 5/17/2021. Accessed January 11, 2024.

Newell-Price, JDC, Auchus RJ. The adrenal cortex. In: Melmed S, Auchus, RJ, Goldfine AB, Koenig RJ, Rosen CJ, eds. Williams Textbook of Endocrinology. 14th ed. Philadelphia, PA: Elsevier; 2020:chap 15.

Review Date 3/12/2024

Updated by: Anna C. Edens Hurst, MD, MS, Associate Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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