RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164066304 T1 Complete Androgen Insensitivity Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164066304 RD 2024/03/28 AB An inherited disorder caused by androgen insensitivity with affected males having a normal male (46,XY) karyotype, but female phenotype with normal female external genitalia and abnormal or absent internal female organs. The testes are often intraabdominal, inguinal, or labial.