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Ideally, a team of health care professionals with expertise in intersex should work together to understand and treat the child with intersex and support the family. Different support groups may differ in their thoughts regarding this very sensitive topic. Endocrine Diseases Read more. People with 5-alpha-reductase deficiency lack the enzyme needed to convert testosterone to dihydrotestosterone DHT. More recently, the opinion of many experts has shifted. There are over different defects that have been identified so far, and each causes a different type of AIS.

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Birth Defects Read more. Approach to the infant with a suspected disorder of sex development. This most often is the result of a female fetus having been exposed to excess male hormones before birth. Most change to external male genitalia around the time of puberty. Look for one that supports your thoughts and feelings on the topic.

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This one may not be noticeable until puberty. Too much aromatase activity can lead to excess estrogen female hormone . too little to 46, XX intersex. In the past, the prevailing opinion was that it was generally best to assign a gender as quickly as possible. The person has the chromosomes of a woman, the ovaries of a woman, but external outside genitals that appear male.

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Description: The person has the chromosomes of a woman, the ovaries of a woman, but external outside genitals that appear male. Disorders of sex development. The person may have XX chromosomes, XY chromosomes, or both. Problems with testosterone formation. Most change to external male genitalia around the time of puberty. Deficiencies in any of these enzymes can result in inadequate testosterone and produce a different syndrome of 46, XY intersex. The labia "lips" or folds of skin of the external female genitals fuse, and the clitoris enlarges to appear like a penis. Please see information on the individual conditions.
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