Clinical and Reproductive Characteristics of Patients with Mixed Gonadal Dysgenesis (45,X/46, XY)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology
Link
https://link.springer.com/content/pdf/10.1007/s13224-021-01448-3.pdf
Reference14 articles.
1. Pan L, Su Z, Song J, Xu W, Liu X, Zhang L, Li S. Multidisciplinary collaboration team of DSD management at Shenzhen Children’s Hospital. Growth data and tumour risk of 32 Chinese children and adolescents with 45, X/46. XY Mosaicism BMC Pediatr. 2019;19(1):143.
2. Cools M, Boter M, van Gurp R, Stoop H, Poddighem P, et al. Impact of the Y-containing cell line on histological differentiation patterns in dysgenetic gonads. Clin Endocrinol. 2007;67:184–92.
3. Ahmed SF, Khwaja O, Hughes IA. The role of a clinical score in the assessment of ambiguous genitalia. BJU Int. 2000;85:120–212.
4. Farrugia MK, Sebire NJ, Achermann JC, Eisawi A, Duffy PG, Mushtaq I. Clinical and gonadal features and early surgical management of 45, X/46, XY and 45, X/47, XYY chromosomal mosaicism presenting with genital anomalies. J Pediatr Urol. 2013;9(2):139–44.
5. Tosson H, Rose SR, Gartner LA. Children with 45, X/46, XY karyotype from birth to adult height. Hom Res Paediatr. 2010;74(3):190–200.
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1. A Rare Cause of Male Infertility: Mixed Gonadal Dysgenesis;ENDOCRINOL RES PRACT;2024
2. Virilization and feminization in an adolescent boy with 45X/46XY DSD due to bilateral gonadoblastomas: A case report;Journal of Pediatric Surgery Case Reports;2024-02
3. Clinical and hormonal characteristics and growth data of 45,X/46,XY mosaicism in 38 Chinese patients;Frontiers in Pediatrics;2023-04-19
4. Genetic control of typical and atypical sex development;Nature Reviews Urology;2023-04-05
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