This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Testicular feminisation

Authoring team

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.


Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.