Literature DB >> 22173178

Clinical features and testicular morphology in patients with Kallmann syndrome.

Hidenori Nishio1, Kentaro Mizuno, Yoshinobu Moritoki, Hideyuki Kamisawa, Yoshiyuki Kojima, Haruo Mizuno, Kenjiro Kohri, Yutaro Hayashi.   

Abstract

Kallmann syndrome (KS) is a genetic disorder characterized by the simultaneous occurrence of idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. Here, we present 3 cases of KS with detailed description. In Case 1, testicular morphology was examined by testicular biopsy, and Leydig cells were examined by immunohistochemistry using antibodies against Ad4BP/SF1. Contrary to our predictions, the present study revealed the presence of Leydig cells in the testis. Testicular morphology in the patients with KS is more varied than expected, and further investigation is required to elucidate hormonal effects on normal testicular development. Copyright Â
© 2012 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22173178     DOI: 10.1016/j.urology.2011.10.032

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  3 in total

1.  Gonadotropin treatment for male partial congenital hypogonadotropic hypogonadism in Chinese patients.

Authors:  Ming Hao; Min Nie; Bing-Qing Yu; Yin-Jie Gao; Xi Wang; Wan-Lu Ma; Qi-Bin Huang; Rui Zhang; Jiang-Feng Mao; Xue-Yan Wu
Journal:  Asian J Androl       Date:  2020 Jul-Aug       Impact factor: 3.285

Review 2.  Update in the evaluation of the azoospermic male.

Authors:  Ahmet Gudeloglu; Sijo J Parekattil
Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365

3.  Efficacy and Outcome Predictors of Gonadotropin Treatment for Male Congenital Hypogonadotropic Hypogonadism: A Retrospective Study of 223 Patients.

Authors:  Zhaoxiang Liu; Jangfeng Mao; Xueyan Wu; Hongli Xu; Xi Wang; Bingkun Huang; Junjie Zheng; Min Nie; Hongbing Zhang
Journal:  Medicine (Baltimore)       Date:  2016-03       Impact factor: 1.889

  3 in total

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