Recurrence of a nonsense mutation in the conserved domain of SRY in a Brazilian patient with 46,XY gonadal dysgenesis

J Pediatr Endocrinol Metab. 1999 May-Jun;12(3):455-7. doi: 10.1515/jpem.1999.12.3.455.

Abstract

We tested a female patient with 46,XY karyotype and pure gonadal dysgenesis for the presence of the SRY gene and for mutations within the SRY conserved domain. A point mutation was identified at nucleotide position 209 with respect to the first ATG. The base substitution is a G-->A transition in the first nucleotide of codon 70 which changes a tryptophan (TGG) to a stop codon (TAG). Even though the father was not available for investigation we assumed that it is a de novo mutation, since it probably generates a nonfunctional truncated protein.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Codon, Nonsense / genetics*
  • DNA / genetics
  • Female
  • Gonadal Dysgenesis, 46,XY / genetics*
  • Gonadal Dysgenesis, 46,XY / surgery
  • Humans
  • Point Mutation / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tryptophan / genetics
  • Tryptophan / metabolism

Substances

  • Codon, Nonsense
  • Tryptophan
  • DNA