Indications for familial screening and gonadectomy in patients with 46,XY gonadal dysgenesis
Author:
Publisher
Wiley
Subject
Obstetrics and Gynecology,General Medicine
Reference5 articles.
1. Complete XY gonadal dysgenesis and aspects of the SRY genotype and gonadal tumor formation;Uehara;J Hum Genet,2002
2. Malignant potential of the dysgenetic gonad: Part 1;Schellhas;Obstet Gynecol,1974
3. Gonadoblastoma: a review of 74 cases;Scully;Cancer,1970
4. Gonadoblastoma in infancy: indications for early gonadectomy in 46XY gonadal dysgenesis;Olsen;J Pediatr Surg,1988
5. Genetic mechanisms that regulate testis determination;Carrillo;Rev Endocr Metab Disord,2004
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2. Familial Swyer Syndrome; Complete Pure Gonadal Dysgenesis in Two Sisters, Manifested as Two Different Clinics and Associated with 46 XY-Karyotype;Journal of Clinical Obstetrics & Gynecology;2022
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4. Dysgerminoma in a Prepubertal Girl with Complete 46XY Gonadal Dysgenesis: Case Report and Review of the Literature;Journal of Pediatric and Adolescent Gynecology;2020-10
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