Congenital no vagina

Congenital no vagina is usually characterized by normal female chromosome karyotype, normal body growth and secondary sexual development in women, normal vulva, vaginal loss, uterine development (only double-angled residual), small fallopian tubes, and normal ovarian development and function Rokitansky-Kustner-Hauser syndrome is most common in patients. Testicular feminization (androgen insensitivity syndrome) is rare. Very few are true bisexual or hypogonadal.