An individual with androgen insensitivity syndrome will:

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An individual with androgen insensitivity syndrome (AIS) is born with male chromosomes and internal testes, but their body does not respond to androgens (male hormones) during fetal development. As a result, the individual's external genitals may appear female or ambiguous. In most cases, individuals with AIS are raised as female and may identify as female. They typically do not develop secondary sex characteristics associated with puberty such as facial hair, a deep voice, and muscle mass. However, they may still be fertile as adults and may have a preference for male or female sexual partners.

An Individual with Androgen Insensitivity Syndrome Will