Familial occurrence of Turner syndrome: casual event or increased risk?

J Pediatr Endocrinol Metab. 2011;24(3-4):223-5. doi: 10.1515/jpem.2011.091.

Abstract

Aim: The prevalence of Turner syndrome (TS) at birth has been estimated as approximately 1 in 2500 live female births. An increased risk of TS in subsequent pregnancies for couples who already have a daughter with TS has not been reported.

Methods: We reviewed the records of 140 patients to evaluate the presence of familial TS occurrence.

Results: Recurrence of TS was observed in 1.4% of our case series, which represents a 35-fold increased probability of having a second child with TS compared to no recurrence.

Conclusion: This observation suggests that a risk of recurrence is possible, even though it is generally assumed that the likelihood of recurrent pregnancies with TS is similar to that in the general population. A wider study would be useful to confirm these data to improve genetic counseling for families with a daughter with TS.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Aberrations
  • Family Health*
  • Female
  • Genetic Counseling
  • Genetic Predisposition to Disease*
  • Humans
  • Infant
  • Risk Factors
  • Siblings
  • Turner Syndrome / genetics*
  • Young Adult