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Correlation Analysis of Genotypes and Phenotypes in Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism.

Frontiers in endocrinology - 1 Jan 2022

Wang Yi, Qin Miao, Fan Lijun, Gong Chunxiu

Abstract excerpt

Congenital hypogonadotropic hypogonadism (CHH) can be divided into Kallmann syndrome (KS) and normosmic HH (nHH). The clinical and genetic characteristics of CHH have been studied in adults, but less in pre-adults. The medical records of patients with CHH in our gonad disease database from 2008 to 2020 were evaluated. In total, 125 patients aged 0 to 18 years were enrolled in our study. KS patients had a higher...

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Child
China
Genotype
Hypogonadism
Kallmann Syndrome
Penis

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PMID: 35669683
DOI: 10.3389/fendo.2022.846801
PMCID: PMC9164197

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