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Androgen insensitivity syndrome is an X-linked recessive condition due to a complete or partial insensitivity to androgen, resulting in a failure of normal masculinisation of the external genitalia in chromosomally male individuals. This failure of virilisation can be either complete or partial depending on the amount of residual androgen receptor function. It is classified into three categories depending upon the degree of genital masculinisation into complete, partial and mild insensitivitydoi:10.18203/2320-1770.ijrcog20150753 fatcat:2a4jyne3crhivewdpb76fkgima