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Androgen insensitivity syndrome (ais) is a rare, inherited, sexual development disorder Androgen insensitivity syndrome (ais) is typically characterized by evidence of feminization (i.e., undermasculinization) of the external genitalia at birth, abnormal secondary. People with ais are genetically male, but don’t develop male external genitals because.
Ais results when the function of the androgen receptor (ar) is impaired Androgen insensitivity syndrome (ais) is an intersex condition in which people who are genetically male experience variations in their sexual and reproductive organs. The ar protein (pictured) mediates the effects of androgens in the human body
Androgen insensitivity syndrome (ais) is a.
In people with androgen insensitivity syndrome, the body's cells and tissues are unable to respond to certain male sex hormones (called androgens) that are important for normal male sexual. Androgen insensitivity syndrome (ais) is when a person who has one x and one y chromosome (typically seen in males) is resistant to hormones that produce a male appearance (called. Androgen insensitivity syndrome (ais) affects the development of a person's genitals and reproductive organs The 2 types of ais are called complete androgen insensitivity syndrome.
Well, that’s easy, you get us If you have ais, all that means is that our body doesn’t understand androgens very well or at all This means that our bodies may.
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