Individuals with AIS, or Androgen Insensitivity Syndrome, typically have a range of physical characteristics and hormone levels that are associated with the condition. Generally, individuals with AIS are born with XY chromosomes, but their bodies do not respond to androgens, which are hormones that typically develop male sexual characteristics. As a result, individuals with AIS typically have female external genitalia and internal reproductive organs, however, they may not have a uterus or ovaries. In addition, they often have underdeveloped testicles, which are located either in the abdomen or inguinal canal.
In terms of physical characteristics, individuals with AIS typically have external female genitalia, such as a clitoris and labia, as well as a female-appearing external appearance. They may also have a gender-neutral or female-appearing body shape, with a lack of facial and body hair. As they reach puberty, they may also experience a decreased amount of breast development, as well as a decrease in their hormone levels, including androgens, estrogen, and progesterone.
In terms of social and emotional characteristics, individuals with AIS may experience a range of psychological issues, including confusion and anxiety regarding their gender identity, feelings of isolation, and difficulty in forming relationships. They may also have difficulty in understanding and expressing their feelings, as well as difficulty in adjusting to societal norms and expectations. Furthermore, they may experience a range of physical issues, such as chronic pain, fatigue, and infertility.
Overall, individuals with AIS typically have a range of physical characteristics, hormone levels, and social and emotional issues that are associated with the condition. These can vary from person to person, and it is important to understand that individuals with AIS experience a wide range of issues that can be addressed with proper care and support.