Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review
Author:
Publisher
Korean Society of Pediatric Endocrinology
Subject
Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
http://e-apem.org/upload/pdf/apem-2040170-085.pdf
Reference30 articles.
1. Androgen insensitivity syndrome
2. Germ Cell Tumors in the Intersex Gonad: Old Paths, New Directions, Moving Frontiers
3. Frequency of gonadal tumours in complete androgen insensitivity syndrome (CAIS): A retrospective case-series analysis
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3. A CASE REPORT OF COMPLETE ANDROGEN INSENSITIVITY SYNDROME RISING A CONCERN ABOUT THE TIME OF SURGERY AND THE ROLE OF PARENTS' BEHAVIOR;Journal of IMAB - Annual Proceeding (Scientific Papers);2024-05-09
4. Androgen Insensitivity Syndrome with Bilateral Gonadal Sertoli Cell Lesions, Sertoli–Leydig Cell Tumor, and Paratesticular Leiomyoma: A Case Report and First Systematic Literature Review;Journal of Clinical Medicine;2024-02-06
5. Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes;Annals of Pediatric Endocrinology & Metabolism;2023-09-30
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