| Literature DB >> 22173178 |
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 ÂEntities:
Mesh:
Year: 2011 PMID: 22173178 DOI: 10.1016/j.urology.2011.10.032
Source DB: PubMed Journal: Urology ISSN: 0090-4295 Impact factor: 2.649