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Androgen-Insensitivity Syndrome (Testicular Feminization)

542  relevant articles (5 outcomes, 51 trials/studies) found for this Disease

Description: A familial form of PSEUDOHERMAPHRODITISM transmitted as an X-linked recessive trait. These patients have a karyotype of 46,XY with end-organ resistance to androgen due to mutations in the androgen receptor (RECEPTORS, ANDROGEN) gene. Severity of the defect in receptor quantity or quality correlates with their phenotypes. In these genetic males, the phenotypic spectrum ranges from those with normal female external genitalia, through those with genital ambiguity as in Reifenstein Syndrome, to that of a normal male with INFERTILITY.

Also Known As:
Testicular Feminization; Reifenstein Syndrome; Reifenstein's Syndrome; Androgen-Insensitivity Syndrome, Complete; Androgen-Insensitivity Syndrome, Partial; Androgen Insensitivity Syndrome; Androgen Insensitivity Syndrome, Complete; Androgen Insensitivity Syndrome, Partial; Androgen-Insensitivity Syndromes, Partial; Reifensteins Syndrome

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Disease Context: Research Results