Someone with Androgen Insensitivity Syndrome (AIS) appears to be like any other person. They are typically born with a female-appearing body, and their physical development will follow a female pattern. However, internally their reproductive system may not be typically female.
AIS is an intersex condition caused by a genetic mutation that makes the body unable to respond to androgen hormones (such as testosterone). This means that while the body may look female on the outside, it is not able to respond to the male hormones that normally cause male development.
Typically, people with AIS will have normal female physical features, and may have some male secondary sex characteristics. For example, they may have a deeper voice than most females, and may have more muscle mass. They may also have some male reproductive organs, such as testes, but they may not be able to produce sperm.
People with AIS may also have some psychological differences from other people. They may have difficulty identifying with either gender, and may feel like they do not fit into either male or female gender roles. They may also feel isolated or different from other people, and may have difficulty forming relationships.
Overall, people with AIS appear to be like any other person, and may have some physical and psychological differences that make them unique. It is important to be respectful and understanding of people with AIS, and to recognize that they are still individuals with their own unique needs and experiences.