Clinical and endocrine correlates of genetic etiologies in severe hypospadias: Study from 34 patients.

Wen-Hua Huang; Ya-Nan Wang; Qian-Qian Tan; Wei Zeng; Xu Cui; Yong Zhou; Chao-Ming Zhou

doi:10.1016/j.jpurol.2026.106111

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Clinical and endocrine correlates of genetic etiologies in severe hypospadias: Study from 34 patients.

Wen-Hua Huang·Ya-Nan Wang·Qian-Qian Tan·Wei Zeng·Xu Cui·Yong Zhou·Chao-Ming Zhou

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Abstract

OBJECTIVE: Hypospadias is a prevalent congenital anomaly (0.3%-1.0%); however, severe hypospadias (defined as proximal cases with the meatus at the penoscrotal junction, scrotum, or perineum) is a rare and clinically challenging entity with a multifactorial etiology. This study aimed to characterize the interrelationships among the clinical, endocrine, and genetic profiles in children with severe hypospadias. MATERIALS AND METHODS: We conducted a comprehensive analysis of 34 male patients with severe hypospadias. Preoperative hormone levels were measured using two methods: chemiluminescent immunoassay for luteinizing hormone and follicle-stimulating hormone, and liquid chromatography-tandem mass spectrometry for testosterone (T), dihydrotestosterone (DHT), dehydroepiandrosterone (DHEA), 17α-hydroxyprogesterone (17α-OHP), and other steroids. Genetic analysis was conducted via whole exome sequencing. RESULTS: The diagnostic yield of clinically relevant genetic variants (including pathogenic and likely pathogenic, and variants of uncertain significance) in our cohort was 41.2% (14/34) of patients. Patients carrying these variants exhibited a more complex phenotypic profile compared to non-carriers, including a significantly higher rate of patients with ≥3 associated malformations and a greater prevalence of cryptorchidism. Furthermore, the group with clinically relevant variants showed selective elevations in adrenal-derived precursors, specifically 17α-OHP and DHEA. Correlation analysis revealed significant positive associations of both 17α-OHP levels and the T/DHT ratio with the number of associated malformations. CONCLUSION: This study reveals significant genetic heterogeneity in patients with severe hypospadias. Those carrying genetic variants was associated with more severe clinical phenotypes, while certain endocrine variations, including the elevation of adrenal-derived hormones, were also observed in this cohort.

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Humans Male Hypospadias Child, Preschool Severity of Illness Index Infant Child 17-Alpha-Hydroxyprogesterone Cryptorchidism Genetics Multiple malformations Journal Article

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Wen-Hua Huang, Ya-Nan Wang, Qian-Qian Tan, Wei Zeng, Xu Cui, Yong Zhou, Chao-Ming Zhou. 2026-06-19. Clinical and endocrine correlates of genetic etiologies in severe hypospadias: Study from 34 patients.. https://doi.org/10.1016/j.jpurol.2026.106111

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Journal Article resource Child subject Child, Preschool subject Humans subject Infant subject Journal Article subject Male subject

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