Androgen-induced hermaphroditism

Androgen-induced hermaphroditism is a medical condition that results from exposure to androgens, which are male sex hormones, during the early stages of fetal development. This condition can lead to the development of both male and female sexual characteristics in the same individual.

Causes

The primary cause of androgen-induced hermaphroditism is the exposure of a fetus to androgens during the early stages of development. This can occur due to a variety of reasons, including the use of certain medications by the mother during pregnancy, or due to certain genetic conditions.

Symptoms

Individuals with androgen-induced hermaphroditism may exhibit a range of symptoms, depending on the extent of their exposure to androgens. These can include the development of both male and female sexual characteristics, such as the presence of both testes and ovaries, or the development of ambiguous genitalia.

Diagnosis

Diagnosis of androgen-induced hermaphroditism can be challenging, as the symptoms can vary widely between individuals. However, it typically involves a combination of physical examination, medical history, and genetic testing.

Treatment

Treatment for androgen-induced hermaphroditism typically involves a combination of hormone therapy and, in some cases, surgery. The goal of treatment is to help the individual live a healthy and fulfilling life, and to manage any physical or psychological symptoms that may arise as a result of the condition.

See also

• Androgen
• Hermaphroditism
• Intersex
• Sexual differentiation

References

Androgen-induced hermaphroditism Resources
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