Case Report

Vol. 25 No. 1 (2021): Endocrinology Research and Practice
DOI: https://doi.org/10.25179/tjem.2020-73399

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Published: Mar 1, 2021
Keywords:
Disorder of sex development; hypergonadotropic; hypogonadism

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Mustafa CAN
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Muhammet KOCABAŞ
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
İlker ÇORDAN
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Hatice ÇALISKAN BURGUCU
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Melia KARAKÖSE
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Mustafa KULAKSIZOĞLU
Division of Endocrinology and Metabolism, Necmettin Erbakan University Meram Faculty of Medicine, Konya, TURKEY
Feridun KARAKURT
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY

SRY-Positive 46-XX Testicular Disorder of Sex Development as a Rare Cause of Male Hypergonadotropic Hypogonadism: A Case Report

Main Article Content

Mustafa CAN
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Muhammet KOCABAŞ
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
İlker ÇORDAN
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Hatice ÇALISKAN BURGUCU
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Melia KARAKÖSE
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY
Mustafa KULAKSIZOĞLU
Division of Endocrinology and Metabolism, Necmettin Erbakan University Meram Faculty of Medicine, Konya, TURKEY
Feridun KARAKURT
Department of Endocrinology and Metabolism, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, TURKEY

Abstract

ABSTRACT



46XX testicular Disorder of Sex Development (DSD) is a rare condition characterized by sexual differentiation disorder with testicular insufficiency. Normal sex development often complicates the diagnosis of this ailment in adults. Patients are usually diagnosed incidentally during infertility research. In this article, we aimed to highlight the hormonal, molecular, and cytogenetic results of an adult male patient diagnosed with 46XX testicular DSD suffering from hypergonadotropic hypogonadism.



 



 


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