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Intersex

What is it?

Intersex is a state where a newborn’s sex orgrans has anatomic characteristics of both sexes, making it impossible to identify the sex of the baby from its outward appearance. Sometimes, the genetic sex (as indicated by chromosomes) may not match the appearance of the sex organs.

Who gets it?

Intersex affects one in every 2,000 births.

What causes it?

Intersex may be caused by any abnormality in chromosomes or sex hormones, or in the unborn baby's response to the hormones. The condition can also be caused by congenital adrenal hyperplasia, a disease that blocks the infant’s metabolism and can cause a range of symptoms, including abnormal sex organs.

What are the symptoms?

An infant with an intersex state can be classified as a true hermaphrodite, a female pseudohermaphrodite, or a male pseudohermaphrodite. A true hermaphrodite is born with both ovaries and testicles and has mixed male and female sex organs. This condition is extremely rare. A female pseudohermaphrodite is a genetic female with external sex organs that look like a penis. A male pseudohermaphrodite is a genetic male with external sex organs that fail to develop normally. Intersex males may have testes and a female-like vulva, or a very small penis.

How is it diagnosed?

When doctors are uncertain about a newborn's sex, a specialist in infant hormonal problems is usually consulted as soon as possible. The specialist may perform an ultrasound to locate a uterus behind the bladder and determine if there is a cervix or uterine canal. Blood tests can check the levels of sex hormones in the baby's blood, and chromosome analysis (called karyotyping) can determine sex. Explorative surgery or a biopsy of reproductive tissue may also be necessary.

What is the treatment?

Treatment of intersex states is controversial. Traditional treatment assigns sex according to test results, the potential for the child to identify with a sex, and the ease of genital surgery to make the organs look more normal. Treatment may then include reconstructive surgery followed by hormone therapy. Babies born with congenital adrenal hyperplasia can be treated with cortisone-type drugs and sometimes surgery. The American Academy of Pediatrics states that these children can be raised successfully as members of either sex, and recommends surgery within the first 15 months of life.

Some people are critical of this approach, including intersex adults who were operated on as children. The remolded genitals do not function sexually and can be the source of lifelong pain. They suggest that surgery be delayed until the patient can make informed choices about surgery and intervention.

Self-care tips

Counseling should be given to the entire family of an intersex newborn, and should also be provided to the child when he or she is old enough.


This information has been designed as a comprehensive and quick reference guide written by our health care reviewers.  The health information written by our authors is intended to be a supplement to the care provided by your physician.  It is not intended nor implied to be a substitute for professional medical advice.

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This page was last updated on October 31, 2006
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