Androgen insensitivity syndrome

Androgen insensitivity syndrome (AIS) is a disorder of sex development (DSD) characterized by the presence of female external genitalia, ambiguous genitalia or variable defects in virilization in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS).

Also known as: AIS, Goldberg-Maxwell syndrome, Morris syndrome, androgen insensitivity syndrome, androgen insensitivity, X-linked recessive, androgen resistance syndrome, testicular feminization syndrome, AR deficiency

6 clinical trials for this condition and its sub-types, 1 tagged with Androgen insensitivity syndrome itself.