Morphological features of female gonadal dysgenesis and karyotype in patients with Shereshevsky-Turner syndrome
- Authors: Kogan E.A.1, Ushakova O.E1, Kur’yanova Y.N2, Fayzullina N.M2, Stupko O.K2
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Affiliations:
- I.M. Sechenov First Moscow State Medical University
- Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology
- Issue: Vol 3, No 2 (2016)
- Pages: 87-91
- Section: Original study articles
- URL: https://journals.rcsi.science/2313-8726/article/view/35309
- DOI: https://doi.org/10.18821/2313-8726-2016-3-2-87-91
- ID: 35309
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##article.viewOnOriginalSite##About the authors
Evgeniya A. Kogan
I.M. Sechenov First Moscow State Medical University
Email: koganevg@gmail.com
MD, PhD, DSci., Professor, Head of the Department of Pathological Anatomy of the I.M. Sechenov First Moscow State Medical University Moscow, 119991, Russian Federation
O. E Ushakova
I.M. Sechenov First Moscow State Medical UniversityMoscow, 119991, Russian Federation
Yu. N Kur’yanova
Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and PerinatologyMoscow, 117997, Russian Federation
N. M Fayzullina
Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and PerinatologyMoscow, 117997, Russian Federation
O. K Stupko
Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and PerinatologyMoscow, 117997, Russian Federation
References
- Кожухарь В.Г. SRY и SOX9 - главные факторы генетической детерминации пола у млекопитающих. Цитология. 2012; 54(5): 390-404.
- Zelaya G., López Marti J.M., Marino R., Garcia de Dávila M.T., Gallego M.S. Gonadoblastoma in patients with Ullrich-Turner syndrome. Pediatr. Dev. Pathol. 2015; 18(2): 117-21.
- Pouresmaeili F., Fazeli Z. Premature ovarian failure: A critical condition in the reproductive potential with various genetic causes. Intern. J. Fertil. Steril. 2014; 8(1): 1-12.
- Zhong Q., Layman L.C. Genetic considerations in the patient with Turner syndrome - 45,X with or without mosaicism. Fertil. and Steril. 2012; 98(4): 775-9.
- Oliveira R.M., Verreschi I.T., Lipay M.V., Eça L.P., Guedes A.D., Bianco B. Y- chromosome in Turner syndrome: review of the literature. Sao Paolo Med. J. 2009; 127(6): 373-8.
- Britt K.L., Saunders P.K., McPherson S.J., Misso M.L., Simpson E.R., Findlay J.K. Estrogen actions on follicle formation and early follicle development. Biol. Reprod. 2004; 71(5): 1712-23.
- Walters K.A., Allan C.M., Handelsman D.J. Androgen actions in the ovary. Biol. Reprod. 2008; 78(3): 380-9.
- Weil S., Vendola K., Zhou J., Bondy C.A. Androgen and Follicle-Stimulating Hormone interactions in primate ovarian follicle development. J. Clin. Endocrinol. Metab. 1999; 84(8): 2951-6.
- Mills S. Е. Histology for Pathologists. USA: Lippincott Williams & Wilkins; 2012.
- Modi D.N., Sane S., Bhartiya D.Accelerated germ cell apoptosis in sex chromosome aneuploid fetal human gonads. Mol. Hum. Reprod. 2003; 9(4): 219-25.
- Wolff D.J., Van Dyke D.L., Powell C.M. Laboratory guideline for Turner syndrome. Genet. Med. 2010; 12 (1): 52-5.
- Blazek N., Kalvaitis K. Hidden Y chromosome mosaicism in 48 Egyptian patients with Turner’s syndrome. Endocr. Today. 2010; 8: 18.
- Juengel J.L., Heath D.A., Quirke L.D., McNatty K.P. Oestrogen receptor alpha and beta, androgen receptor and progesterone receptor mRNA and protein localisation within the developing ovary and in small growing follicles of sheep. Reproduction. 2006; 131(1): 81-92.
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