Complete androgen insensitivity syndrome in a 13-year-old Lebanese child, reared as female, with bilateral inguinal hernia: a case report

被引:0
作者
Stephanie Farah
Dana El Masri
Kamal Hirbli
机构
[1] American University Medical Center,Department of Endocrinology, Diabetes and Metabolism. Lebanese
[2] LAUMCRH,undefined
来源
Journal of Medical Case Reports | / 15卷
关键词
Androgen insensitivity syndrome; Amenorrhea; Inguinal hernia; Case report;
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[1]  
Hughes IA(2006)Androgen resistance Best Pract Res Clin Endocrinol Metab. 20 577-598
[2]  
Deeb A(2009)Clinical findings in prepubertal girls with inguinal hernia with special reference to the diagnosis of androgen insensitivity syndrome Scand J Urol Nephrol. 43 42-46
[3]  
Hurme T(2005)Coexistence of Kallmann syndrome and complete androgen insensitivity in the same patient Eur J Endocrinol. 152 813-817
[4]  
Lahdes-Vasama T(2001)Molecular basis of androgen insensitivity Mol Cell Endocrinol. 179 105-9
[5]  
Makela E(2006)Consensus statement on management of intersex disorders Arch Dis Child 91 554-321
[6]  
Iber T(1995)Androgen receptor defects: historical, clinical, and molecular perspectives Endocr Rev. 16 271-580
[7]  
Toppari J(2015)Androgen insensitivity syndrome Best Pract Res Clin Endocrinol Metab. 29 569-310
[8]  
Gannagé-Yared MH(2012)Male patients with partial androgen insensitivity syndrome: a longitudinal follow-up of growth, reproductive hormones and the development of gynaecomastia Arch Dis Child 97 403-86
[9]  
Dodé C(2008)Complete androgen insensitivity syndrome—a review J Pediatr Adolesc Gynecol. 21 305-822
[10]  
Ghanem I(1962)Apparent female infants with hernias and testes Am J Dis Child. 104 82-403