Phenotype and genetic characteristics in 20 Chinese patients with 46,XY disorders of sex development

Purpose46,XY disorders of sex development (DSD) is the most complicated and common type of DSD. To date, more than 30 genes have been identified associated with 46,XY DSD. However, the mutation spectrum of 46,XY DSD is incomplete owing to the high genetic and clinical heterogeneity. This study aims to provide clinical and mutational characteristics of 18 Chinese patients with 46,XY DSD.MethodsA total of 20 unrelated individuals with 46,XY DSD were recruited. Whole-exome sequencing (WES) or custom-panel sequencing combined Sanger sequencing were performed to detect the pathogenic mutations. The pathogenicity of the variant was assessed according to the American College of Medical Genetics and Genomics (ACMG) guidance and technical standards recommended by the ACMG and the Clinical Genome Resource (ClinGen).ResultsSix patients harbored NR5A1 mutations; two patients harbored NR0B1 mutations; six patients harbored SRD5A2 mutations; six patients harbored AR mutations. Six novel genetic variants were identified involved in three genes (NR5A1, NR0B1, and AR).ConclusionWe determined the genetic etiology for all enrolled patients. Our study expanded the mutation spectrum of 46,XY DSD and provided diagnostic evidence for patients with the same mutation in the future.

Automated summary

This study investigated the clinical and mutational characteristics of 18 Chinese patients with 46,XY disorders of sex development (DSD). The results revealed six NR5A1 mutations, two NR0B1 mutations, six SRD5A2 mutations, and six AR mutations among the patients. Additionally, six novel genetic variants involving three genes (NR5A1, NR0B1, and AR) were identified.