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Testicular feminisation

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

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These are individuals which are genotypically male with a 46XY karyotype, but phenotypically are female. The condition results from a complete or partial absence of cytoplasmic receptors for testosterone in target tissues. It is an X-linked disorder with an incidence of 1 in 62000 male births.

The feminisation is a consequence of increased testicular secretion of oestradiol and from peripheral conversion of androgens to oestradiol. Serum LH and FSH are elevated as testosterone is ineffective at the hypothalamus.


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