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SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.

Flávia Marcorin de OliveiraBeatriz Amstalden BarrosAna Paula Dos SantosNilma Lúcia Viguetti CamposTaís Nitsch MazzolaPaulo Latuf FilhoLiliana Aparecida Lucci De Angelo AndradeMara Sanches GuaragnaMaricilda Palandi de MelloGil Guerra-JuniorTársis Antonio Paiva VieiraAndréa Trevas Maciel-Guerra
Published in: American journal of medical genetics. Part A (2022)
Ovotesticular disorders of sex development (OT-DSD) are characterized by ovarian follicles and seminiferous tubules in the same individual, with a wide range of atypical genitalia. We report on two sibs with atypical genitalia and SRY-negative 46,XX DSD, OT-DSD was confirmed only in the boy, while the girl had bilateral ovaries. Chromosome microarray analysis (CMA) showed a 737-kb duplication at Xq27.1 including the entire SOX3 gene in both sibs, which was confirmed by quantitative real time PCR. Also, X chromosome inactivation assay showed random inactivation in both sibs. Whole exome sequencing revealed no pathogenic or likely pathogenic variant. CMA of the parents showed normal results for both, suggesting that germline mosaicism could be the reason of recurrence of this duplication in the siblings. Our results support a pathogenic role of SOX3 overexpression in 46,XX subjects leading to variable DSD phenotypes.
Keyphrases
  • transcription factor
  • stem cells
  • real time pcr
  • copy number
  • dna repair
  • cell proliferation
  • high resolution
  • high throughput
  • genome wide identification
  • genome wide
  • gene expression
  • oxidative stress
  • mass spectrometry