Whole-exome sequencing analysis of idiopathic hypogonadotropic hypogonadism: comparison of varicocele and non-obstructive azoospermia

Abstract excerpt

<h4>Background: </h4> As a rare disease leading to male infertility, A has strong heterogeneity of clinical phenotype and gene mutation. At present, there is no effective diagnosis and treatment method for this disease, and the research on its pathogenesis is not exhaustive Objectives To explore the possible new pathogenic gene of idiopathic hypogonadotrophic hypogonadism and the pathological mechanism affecting...

Topics

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• Azoospermia
• Exome Sequencing
• Hypogonadism
• Kallmann Syndrome
• Mutation
• Mutation, Missense
• Receptor, Fibroblast Growth Factor, Type 1
• Young Adult

Identifiers and source

Literature Corpus work

8e46d1b1-d2c7-548a-b0ab-90987b25b1a3

DOI

10.21203/rs.3.rs-2605075/v1