Literature DB >> 33419659

Kallman syndrome and central non-obstructive azoospermia.

Sameer Thakker1, Jesse Persily1, Bobby B Najari2.   

Abstract

The understanding of male factors of infertility has grown exponentially in the past ten years. While clear guidelines for obstructive azoospermia have been developed, management of non-obstructive azoospermia has lagged. Specifically, management of Kallmann Syndrome and central non-obstructive azoospermia has been limited by a lack of understanding of the molecular pathogenesis and investigational trials exploring the best option for management and fertility in these patients. This review aims to summarize our current understanding of the causes of central hypogonadotropic hypogonadism with a focus on genetic etiologies while also discussing options that endocrinologists and urologists can utilize to successfully treat this group of infertile men. Published by Elsevier Ltd.

Entities:  

Keywords:  Kallman syndrome; congenital hypogonadotropic hypogonadism; fertility; genetics; non-obstructive azoospermia

Mesh:

Year:  2020        PMID: 33419659     DOI: 10.1016/j.beem.2020.101475

Source DB:  PubMed          Journal:  Best Pract Res Clin Endocrinol Metab        ISSN: 1521-690X            Impact factor:   4.690


  2 in total

Review 1.  The Fate of Leydig Cells in Men with Spermatogenic Failure.

Authors:  Daria Adamczewska; Jolanta Słowikowska-Hilczer; Renata Walczak-Jędrzejowska
Journal:  Life (Basel)       Date:  2022-04-12

2.  Molecular diagnosis of Kallmann syndrome with diabetes by whole exome sequencing and bioinformatic approaches.

Authors:  Shuang-Shuang Sun; Rui-Xue Wang
Journal:  World J Diabetes       Date:  2021-12-15
  2 in total

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