Lee PA, Houk CP, Ahmed SF, Hughes IA; International Consensus Conference on Intersex organized by the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. Consensus statement on management of intersex disorders. Pediatrics 2006;118:e488–500.PubMedCrossrefGoogle Scholar
Tayel SM, Ismael H, Kandil H, Abd Rabuh A, Sallam H. Congenital adrenal hyperplasia in Alexandria, Egypt: a high prevalence justifying the need for a community-based newborn screening program. J Trop Pediatr 2011;57:232–4.CrossrefWeb of SciencePubMedGoogle Scholar
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2010;95:4133–60.PubMedCrossrefWeb of ScienceGoogle Scholar
Ahmed SF, Cheng L, Dovey JR, Hawkins JR, Martin H, et al. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome. J Clin Endocrinol Metab 2000;85:658–65.PubMedGoogle Scholar
Mao Y, Chen S, Wang R, Wang X, Qin D, et al. Evaluation and treatment for ovotesticular disorder of sex development (OT-DSD) – experience based on a Chinese series. BMC Urol 2017;17:21.PubMedWeb of ScienceCrossrefGoogle Scholar
Ganie Y, Aldous C, Balakrishna Y. The spectrum of ovotesticular disorders of sex development in South Africa: a single-centre experience. Horm Res Paediatr 2017;87:307–14.Web of ScienceCrossrefPubMedGoogle Scholar
Deeb A, Mason C, Lee YS, Hughes IA. Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome. Clin Endocrinol 2005;63:56–62.CrossrefGoogle Scholar
Johannsen TH, Ripa PL, Mortensen EL, Main KM. Quality of life in 70 women with disorders of sex development. Europ J Endocrinol 2006;155:977–85.Google Scholar
Jürgensen M, Kleinemeier E, Lux A, Steensma TD, Cohen-Kettenis PT, et al. DSD Network Working Group. Psychosexual development in adolescents and adults with disorders of sex development: results from the German Clinical Evaluation Study. J Sex Med 2012;10:2703–14.Google Scholar
Hamza R, Deeb A, Habeb A. Fourth Arab Society for Pediatric Endocrinology and Diabetes (ASPED) – European Society of Paediatric Endocrinology (ESPE) School, 14-17th Dec. 2017, Abu Dhabi, United Arab Emirates. J Rare Disord Diagn Ther 2018;4(S1):9.Google Scholar
Clayton PE, Miller WL, Oberfield SE, Ritzén EM, Sippell WG, et al. Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society. Horm Res 2002;58:188–95.PubMedGoogle Scholar
Meyer-Bahlburg HF, Dolezal C, Baker SW, Ehrhardt AA, New MI. Gender development in women with congenital adrenal hyperplasia as a function of disorder severity. Arch Sex Behav 2006;35:667–84.CrossrefPubMedGoogle Scholar
Houk CP, Lee PA. Approach to assigning gender in 46,XX congenital adrenal hyperplasia with male external genitalia: replacing dogmatism with pragmatism. J Clin Endocrinol Metab 2010;95:4501–8.PubMedWeb of ScienceCrossrefGoogle Scholar
Kulshreshtha B, Philibert P, Eunice M, Khandelwal SK, Mehta M, et al. Apparent male gender identity in a patient with complete androgen insensitivity syndrome. Arch Sex Behav 2009;38:873–5.CrossrefWeb of ScienceGoogle Scholar
Herdt GH, Davidson J. The Sambia “turnim-man”: sociocultural and clinical aspects of gender formation in male pseudohermaphrodites with 5-α-reductase deficiency in Papua New Guinea. Arch Sex Behav 1988;17:33–56.PubMedCrossrefGoogle Scholar
Byers HM, Mohnach LH, Fechner PY, Chen M, Thomas IH, et al. Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5-α reductase type 2 deficiency. Am J Med Genet C Semin Med Genet 2017;175:260–7.CrossrefPubMedGoogle Scholar
Mouriquand PD, Gorduza DB, Gay CL, Meyer-Bahlburg HF, Baker L, et al. Surgery in disorders of sex development (DSD) with a gender issue: if (why), when, and how? J Pediatr Urol J 2016;12:139–49.CrossrefGoogle Scholar
Mouriquand P, Caldamone A, Malone P, Frank JD, Hoebeke P. The ESPU/SPU standpoint on the surgical management of disorders of sex development (DSD). J Pediatr Urol 2014;10:8–10.Web of SciencePubMedCrossrefGoogle Scholar
Creighton S, Chernausek SD, Romao R, Ransley P, Salle JP. Timing and nature of reconstructive surgery for disorders of sex development – introduction. J Pediatr Urol 2012;8:602–10.Web of ScienceCrossrefPubMedGoogle Scholar
Costa EM, Domenice S, Sircili MH, Inacio M, Mendonca BB. DSD due to 5α-reductase 2 deficiency – from diagnosis to long term outcome. Semin Reprod Med 2012;30:427–31.CrossrefWeb of ScienceGoogle Scholar
Khadilkar KS, Budyal SR, Kasaliwal R, Sathe PA, Kandalkar B, et al. Ovotesticular disorder of sex development: a single-center experience. Endocr Pract 2015;21:770–6.Web of ScienceCrossrefPubMedGoogle Scholar
About the article
Published Online: 2019-01-10
Published in Print: 2019-01-28
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organisation(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
Funding: No fund is sought to undertake the study.
Conflict of interest: None to declare.