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2012 | 7 | 6 | 729-732
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Complete androgen insensitivity syndrome: Review of four cases

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1 - 12 - 2012
11 - 10 - 2012
  • [1] Oakes M.B., Eyvazzadeh A.D., Quint E., Smith Y.R., Complete androgen insensitivity syndrome - a review. J Pediatr Adolesc Gynecol 2008; 1: 305–310[WoS][Crossref]
  • [2] Gurer I.E., Demirkiran A.E., Sare M., Sertoly Cell Tumor in Two Sibs with Testicular Feminization Syndrome. Turk J Med Sci 2000; 30: 385–387
  • [3] Gallagher M.P., Oberfield S.E., Disorders of sexual differentiation, In: Peskovitz O.H., Eugster E.A. (Eds.), Pediatric endocrinology: Mechanisms, Manifestations, and management, Lippincott Williams&Wilkins, Philadelphia, 2004, Pp: 243–254
  • [4] Ahmed S.F., Cheng A., Dovey L., Hawkins R.J., Martin H., Rowland J., et al., Phenotypic features, androgen receptor binding, and mutation analysis in 278 clinical cases reported as androgen insensitivity syndrome. J Clin Endocrinol Metab 2000; 85: 658–865[Crossref]
  • [5] Morris J.M., The syndrome of testicular feminization in male pseudohermaphrodities. Am J Obstet Gynec 1953; 65: 1192–1211
  • [6] Deeb A., Hughes I.A., Inguinal hernia in female infants: a cue to check the sex chromosomes? BJU Int 2005; 96: 401–403[Crossref]
  • [7] Selby D.M., Sexual Maldevelopment Syndromes, In: Stocker T., Dehner L.P. (Eds.), Pediatric Pathology, Lippincott Company, Philadephia, 1992; Pp:141–142
  • [8] Alvarez N.R., Lee T.M., Solorzano C.C., Complete androgen insensitivity syndrome: the role of the endocrine surgeon. Am Surg 2005; 71: 241–243 [PubMed]
  • [9] O’Conell M.J., Ramsey H.E., Whang-Peng J., Wiernik P.H., Testicular feminization syndrome in three sibs: emphasis on gonadal neoplasia. Am J Med Sci 1973; 265: 321–333[Crossref]
  • [10] Nojima M., Takeshi T., Ando Y., Musha Y., Kobayashi Y., Ikeda N., et al, Huge seminoma developed in a patient with testicular feminization. J Obstet Gynaecol Res 2004; 30: 109–112[Crossref]
  • [11] Casellato S., Gazzano G., Musi G., Spinelli M., Carmignani L., Rocco F., et al, First case of bilateral intratubular germ cell tumor in androgen insensitivity syndrome. Arch Ital Androl 2007; 79: 135–137
  • [12] Sills E.S., Perloe M., Kalpan C.R., Schlegel P.N., Palermo G.D., Bilateral orchiectomy for the surgical treatment of complete androgen insensitivity syndrome: patient outcome after 1 year of followup. J Laparoendosc Adv Surg Tech A 2003; 13: 193–197[Crossref]
  • [13] Ramani P., Yeung C.K., Habeebu S.S., Testicular intratubular germ cell neoplasia in children and adolescents with intersex. Am J Surg Pathol 1993; 17: 1124–1133[Crossref]
  • [14] Kravarusic D., Seguier-Lipszic E., Feigin E., Nimri R., Nagelberg N., Freude E., Androgen insensitivity syndrome: Risk of malignancy and timing of surgery in paediatric and adolescent population. Afr J Paediatr Surg 2011; 8: 194–198[Crossref]
  • [15] Dènes F.T., Cocuzza M.A., Schneider-Monteiro E.D., Silva F.A., Costa E.M., Mendonca B.B., Arap S., The laparoscopic management of intersex disorders: The preferred approach. BJU Int 2005; 95: 863–867[Crossref]
  • [16] Bonilla-Musoles F., Kushner-Dávalos L., Raga F., Machado L.e., Osborne N.G., Androgen insensitivity syndrome: in utero diagnosis by four-dimensional sonography and amniotic fluid karyotype. J Clin Ultrasound 2006; 34: 30–32[Crossref]
  • [17] Bianca S., Cataliotti A., Bartoloni G., Torrente I., Barrano B., Boemi G., et al. Prenatal Diagnosis of Androgen Insensitivity Syndrome. Fetal Diagn Ther 2009; 26: 167–169[WoS][Crossref]
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