Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal Hyperplasia, and Triple Translocation: Is a Consequence or Coincidence?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,Oncology
Link
https://link.springer.com/content/pdf/10.1007/s12029-020-00408-w.pdf
Reference22 articles.
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2. Nordenstrom A, Falhammar H. Diagnosis and management of the patient with non-classic CAH due to 21-hydroxylase deficiency. Eur J Endocrinol. 2018. https://doi.org/10.1530/EJE-18-0712.
3. Arlt W, Willis DS, Wild SH, Krone N, Doherty EJ, Hahner S, et al. Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients. J Clin Endocrinol Metab. 2010;95:5110–21. https://doi.org/10.1210/jc.2010-0917.
4. Faraj G, Di Gregorio S, Misiunas A, Faure EN, Villabrile P, Stringa I, et al. Virilizing ovarian tumor of cell tumor type not otherwise specified: a case report. Gynecol Endocrinol. 1998;12:347–52.
5. Khosla D, Dimri K, Pandey AK, Mahajan R, Trehan R. Ovarian granulosa cell tumor: clinical features, treatment, outcome, and prognostic factors. N Am J Med Sci. 2014;6:133–8. https://doi.org/10.4103/1947-2714.128475.
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