69. Partial Androgen Insensitivity Syndrome Without Virilization at Puberty: a Case Report

Partial androgen insensitivity syndrome (PAIS), an X-linked genetic disease, varies in phenotype from ambiguous genitalia at birth to normal male genitalia. PAIS patients who have not had gonadectomies tend to have some degree of virilization during puberty with increasing testosterone levels. We present a case of a patient with PAIS who developed female secondary characteristics without virilization at the onset of puberty despite increased testosterone level.