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Korean Journal of Obstetrics and Gynecology ; : 986-989, 2001.
Article Dans Coréen | WPRIM | ID: wpr-98015

Résumé

The Complete testicular feminization syndrome is a hereditary syndrome characterized clinically by female phenotype with 46, XY karyotype and bilateral testes. There is a congenital insensitivity to androgens, transmitted by means of a maternal X-linked recessive gene responsible for the androgen intracellular receptor. Therefore, androgen induction of Wolffian duct development does not occur. However, anti-mullerian hormone activity is present and the individual does not have mullerian development. Principle of treatment is reinforced to live normal female life. This is a case report of testicular feminization syndrome with rudimentary salpinx with the brief review of literatures.


Sujets)
Femelle , Humains , Mâle , Syndrome d'insensibilité aux androgènes , Androgènes , Hormone antimullérienne , Trompes utérines , Gènes récessifs , Caryotype , Phénotype , Testicule , Canaux de Wolff
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