Pseudohermaphroditism
(Redirected from Male pseudohermaphroditism)
Pseudohermaphroditism is a medical condition in which an individual is born with primary sex characteristics of one sex but develops the secondary sex characteristics of the opposite sex. This condition is different from true hermaphroditism, in which an individual has both ovarian and testicular tissue.
Causes[edit | edit source]
Pseudohermaphroditism can be caused by a number of factors, including genetic disorders, hormonal imbalances, and exposure to certain drugs or chemicals in utero. The most common cause is a disorder of sex development (DSD), which can result in ambiguous genitalia and other physical characteristics that do not match the individual's genetic or chromosomal sex.
Types[edit | edit source]
There are two main types of pseudohermaphroditism: male and female.
- Male pseudohermaphroditism is a condition in which an individual has a male XY karyotype, but their external genitalia appear female or ambiguous. This can be caused by a lack of response to androgens, the hormones that promote male sexual development.
- Female pseudohermaphroditism is a condition in which an individual has a female XX karyotype, but their external genitalia appear male or ambiguous. This can be caused by exposure to excess androgens in utero.
Diagnosis[edit | edit source]
Diagnosis of pseudohermaphroditism can be complex and often involves a combination of physical examination, genetic testing, and hormone testing. In some cases, the condition may not be diagnosed until puberty, when the individual develops unexpected secondary sex characteristics.
Treatment[edit | edit source]
Treatment for pseudohermaphroditism depends on the underlying cause and the individual's personal preferences. It may include hormone therapy, surgery, and/or psychological counseling. It's important for individuals with this condition to receive support and understanding from their healthcare providers, family, and community.
See also[edit | edit source]
- Intersex
- Disorders of sex development
- Androgen insensitivity syndrome
- Congenital adrenal hyperplasia
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