Ridley's The Vulva. Группа авторов
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Turner Syndrome Support Society
Turner Syndrome Society of the United States
Disorders of sexual differentiation
MRKH UK
Congenital adrenal hyperplasia
Last accessed September 2021.
References
1 2 Biason‐Lauber, A. WnT4, RSPO1 and FoxL2 in sex development. Semin Reprod Med. 2012; 30(5): 387–395.
2 3 Wilhelm, D., Palmer, S. and Koopman, P. Sex determination and gonadal development in mammals. Physiol Rev. 2007; 87: 1–28.
3 4 Mullen, R.D. and Behringer, R.R. Molecular genetics of Mullerian duct formation, regression and differentiation. Sex Dev. 2014; 8: 281–296.
4 5 Sajjad, Y. Development of the genital ducts and external genitalia in the early human embryo. J Obstet Gynecol Res. 2010; 36: 929–937.
5 6 O’Rahilly, R. and Muller, F. Developmental Stages in Human Embryos. 1987. Carnegie Institution of Washington, Washington DC.
6 18 Cunha, G.R., Cao, T.K., Shen, M. and Robboy, S.L. Molecular mechanisms of development of the human fetal female reproductive tract. Differentiation. 2017; 97: 54–72.
7 19 Robboy, S.J., Karita, T., Baskin, L. and Cunha, G.R. New insights into human female reproductive tract development. Differentiation. 2017; 97: 9–22.
8 21 Witchel, S.F. Disorders of sex development. Best Pract Res Clin Obstet Gynecol. 2018; 48: 90–102.
9 22 Creighton, S., Chernausek, S.D., Romao, R. et al. Timing and nature of reconstructive surgery for disorders of sex development. J Paediatr Urol. 2012; 8: 602–610.
10 23 Ahmed, S.F., Achermann, J.C., Avit, W. et al. Society for Endocrinology UK guidance on the initial evaluation of an infant or adolescent with a suspected disorder of sexual development (Revised 2015). Clin Endocrinol. 2016; 84(5): 771–788.
11 24 Hughes, I.A. Disorders of sexual development: New definition and classification. Best Pract Res Clin Endocrinol Metab. 2008; 22: 119–134.
12 26 Mavridi, A., Ntali, G., Theodora, M. et al. A spontaneous pregnancy in a patient with Turner syndrome with 45,X/47,XXX mosaicism: A case report and review of the literature. J Pediatr Adolesc Gynecol. 2018; 31(6): 651–654.
13 27 Gravholt, C.H., Viuff, M.H., Brun, S. et al. Turner syndrome: Mechanisms and management. Nat Rev Endocrinol. 2019; 15(10): 601–614.
14 28 Gravholt, C.H., Andersen, N.H., Conway, G.S. et al. Clinical practice guidelines for the care of girls and women with Turner syndrome: Proceedings from the 2016 Cincinnati International Turner Syndrome Meeting. Eur J Endocrinol. 2017; 177(3): G1–G70.
15 29 Schoemaker, M.J., Swerdlow, A.J., Higgins, C.D. et al. Cancer incidence in women with Turner syndrome in Great Britain: A national cohort study. Lancet Oncol. 2008; 9: 239–246.
16 30 Matsumoto, F., Matsuyama, S., Matsui, F. et al. Variation of Gonadal dysgenesis and Tumor risk in patients with 45,X/46, XY mosaicism. Urology. 2020; 137: 157–160.
17 33 Falhammar, H., Frisén, L., Hirschberg, A.L. et al. Increased cardiovascular and metabolic morbidity in patients with 21‐hydroxylase deficiency: A Swedish population‐Based National Cohort Study. J Clin Endocrinol Metab. 2015; 100(9): 3520–3528.
18 36 Conlon, J.L. Diethylstilbestrol: Potential health risks for women exposed in utero and their offspring. JAAPA. 2017; 30(2): 49–52.
19 37 Brunskill, P.J. The effects of fetal exposure to danazol. Br J Obstet Gynaecol. 1992; 99(3): 212–215.
20 39 Xue, M., Wang, X., Li, C. et al. Novel pathogenic mutations in disorders of sex development associated genes cause 46,XY complete gonadal dysgenesis. Gene. 2019; 718: 144072.
21 42 Oppelt, P.G., Lermann, J., Strick, R. et al. Malformations in a cohort of 284 women with Mayer‐Rokitansky‐Küster‐Hauser (MRKH) syndrome. Reprod Biol Endocrinol. 2012; 10: 57.
22 43 Rall, K., Eisenbeis, S., Henninger, V. et al. Typical and atypical associated findings in a group of 346 patients with Mayer‐Rokitansky‐Küster‐Hauser syndrome. J Pediatr Adolesc Gynecol. 2015; 28(5): 362–368.
23 44 Fontana, L., Gentilin, B., Fedele, L. et al. Genetics of Mayer‐Rokitansky‐Küster‐Hauser (MRKH) syndrome. Clin Genet. 2017; 91(2): 233‐246.
24 45 Backhouse, B., Hanna, C., Roberska, G. et al. Identification of candidate genes for Mayer‐Rokitansky‐Küster‐Hauser syndrome using genomic approaches. Sex Dev. 2019; 13(1): 26–34.
25 46 ACOG Committee Opinion No 728. Müllerian agenesis: Diagnosis, management, and treatment. Obstet Gynecol. 2018; 131(1): e35–42.
26 48 Edmonds, D.K. Congenital malformations of the genital tract and their management. Best Pract Res Clin Obstet Gynaecol. 2003; 17: 19–40.
27 55 Slavotinek, A.M. and Biesecker, L.G. Phenotypic overlap of McKusick‐Kaufman syndrome with Bardet‐Biedl syndrome: A literature review. Am J Med Genet. 2000; 95: 208–215.
28 72 Woo, L.L., Thomas, J.C., and Brock, J.W. Cloacal exstrophy: A comprehensive review of an uncommon problem. J Pediatr Urol. 2010; 6(2): 102–111.
29 73 Kubota, M., Osuga, Y., Kato, K. et al. Treatment guidelines for persistent cloaca, cloacal exstrophy and Mayer‐Rokitansky‐Küster‐Hauser syndrome for the appropriate transitional care of the patient. Surg Today. 2019; 49(12): 985–1002.
2 The Normal Vulva
Fiona M. Lewis
CHAPTER MENU
Normal vulval anatomy Mons pubis Labia majora Labia minora Sebaceous glands (Fordyce spots) The clitoris