CLC Number: 

  • R699.7
[1] Becker RE, Akhavan A. Prophylactic bilateral gonadectomy for ovotesticular disorder of sex development in a patient with mosaic 45,X/46,X,idic(Y)q11.222 karyotype[J]. Urol Case Rep, 2016, 5: 13-16. doi: 10.1016/j.eucr.2015.12.003.
[2] Kim HI, Lee I, Kim SH, et al. Ovotesticular disorder of sex development in Korean children: a single-center analysis over a 30-year period[J]. J Pediatr Adolesc Gynecol, 2021, 34(5): 626-630.
[3] Melardi JW, Cunha D, Steinmetz L, et al. Puberty in patients with ovotesticular DSD: evaluation of 20 patients and review of the literature[J]. Pediatr Endocrinol Rev, 2020, 17(3): 243-249.
[4] Acién P, Acién M. Disorders of sex development: classification, review, and impact on fertility[J]. J Clin Med, 2020, 9(11): 3555. doi: 10.3390/jcm9113555.
[5] Tachon G, Lefort G, Puechberty J, et al. Discordant sex in monozygotic XXY/XX twins: a case report[J]. Hum Reprod, 2014, 29(12): 2814-2820.
[6] Takahashi K, Sato T, Nishiyama M, et al. Monochorionic diamniotic twins of discordant external genitalia with 45,X/46,XY mosaicism[J]. Mol Genet Genomic Med, 2020, 8(9): e1382. doi: 10.1002/mgg3.1382.
[7] He M, Pepperell JR, Gundogan F, et al. Monochorionic twins discordant for mosaic trisomy 14[J]. Am J Med Genet A, 2014, 164A(5): 1227-1233.
[8] Uehara E, Hattori A, Shima H, et al. Unbalanced Y;7 translocation between two low-similarity sequences leading to SRY-positive 45,X testicular disorders of sex development[J]. Cytogenet Genome Res, 2019, 158(3): 115-120.
[9] McElreavey K, Cortes LS. X-Y translocations and sex differentiation[J]. Semin Reprod Med, 2001,19(2): 133-139.
[10] Margarit E, Coll MD, Oliva R, et al. SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite[J]. Am J Med Genet, 2000, 90(1): 25-28.
[11] Hattori A, Fukami M. Nuclear receptor gene variants underlying disorders/differences of sex development through abnormal testicular development[J]. Biomolecules, 2023, 13(4): 691. doi: 10.3390/biom13040691.
[12] Kremen J, Chan YM. Genetic evaluation of disorders of sex development: current practice and novel gene discovery[J]. Curr Opin Endocrinol Diabetes Obes, 2019, 26(1): 54-59.
[13] Syryn H, Van De Vijver K, Cools M. Ovotesticular difference of sex development: genetic background, histological features, and clinical management[J]. Horm Res Paediatr, 2023, 96(2): 180-189.
[14] Nagaraja MR, Gubbala SP, Delphine SC, et al. Molecular diagnostics of disorders of sexual development: an Indian survey and systems biology perspective[J]. Syst Biol Reprod Med, 2019, 65(2): 105-120.
[15] Chen CQ, Liu Z, Lu YS, et al. True hermaphroditism with dysgerminoma: a case report[J]. Medicine(Baltimore), 2020, 99(22): e20472. doi: 10.1097/MD.0000000000020472.
[16] Khadilkar KS, Budyal SR, Kasaliwal R, et al. Ovotesticular disorder of sex development: a single-center experience[J]. Endocr Pract, 2015, 21(7): 770-776.
[17] Ganie Y, Aldous C, Balakrishna Y, et al. The spectrum of ovotesticular disorders of sex development in South Africa: a single-centre experience[J]. Horm Res Paediatr, 2017, 87(5): 307-314.
[18] Sircili MH, Denes FT, Costa EM, et al. Long-term followup of a large cohort of patients with ovotesticular disorder of sex development[J]. J Urol, 2014, 191(5 Suppl): 1532-1536.
[19] Scarpa MG, Lesma A, Di Grazia M, et al. Ovotesticular differences of sex development: male or female? Case series[J]. Ital J Pediatr, 2019, 45(1): 66. doi: 10.1186/s13052-019-0660-8.
[20] 周大鹏,荆翌峰,韩邦旻,等.真两性畸形伴隐睾原位生殖细胞肿瘤合并性腺母细胞瘤1例报告并文献复习[J]. 中国男科学杂志, 2020, 34(3): 51-53. ZHOU Dapeng, JING Yifeng, HAN Bangmin, et al. Cryptorchidism in true hermaphroditism with a combination of germ cell neoplasia in situ(GCNIS)with gonadoblastoma: a case report and literature review[J]. Chinese Journal of Andrology, 2020, 34(3): 51-53.
[21] 张璞,邓新粮,肖松舒.宫腹腔镜诊治46,XY真两性畸形2例分析[J].现代妇产科进展, 2014, 23(12): 1022-1023. ZHANG Pu, DENG Xinliang, XIAO Songshu. Analysis of 2 cases of 46,XY true hermaphroditism diagnosed and treated by uterine laparoscopy[J]. Progress in Modern Obstetrics and Gynecology, 2014, 23(12): 1022-1023.
[22] 沈莎莎,薛凤麟,常雯,等.真两性畸形并腹股沟副中肾管囊肿1例[J].中国医学影像技术, 2019, 35(3): 346. SHEN Shasha, XUE Fenglin, CHANG Wen, et al. A case of true hermaphrodite combined with inguinal paramesonephric duct cyst[J]. Chinese Medical Imaging Technology, 2019, 35(3): 346.
[23] Shi S, Tang M, Li W, et al. True hermaphroditism with sex cord tumor with annular tubules(SCTAT): a rare case report and review of the literature[J]. BMC Womens Health, 2022, 22(1): 551. doi: 10.1186/s12905-022-02137-7.
[24] Ahmad A, Ayub F, Saleem I, et al. Initial assessment of a child with suspected disorder of sex development[J]. J Pak Med Assoc, 2019, 69(5): 711-717.
[25] 裴顺祥,姜佳星,赵国亮,等.真两性畸形青春期纠正1例[J].中国男科学杂志, 2008, 22(6): 53. PEI Shunxiang, JIANG Jiaxing, ZHAO Guoliang, et al. A case of correction of true hermaphroditism during puberty[J]. Chinese Journal of Andrology, 2008, 22(6): 53.
No related articles found!
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!