Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studies

Am J Med Genet. 1992;43(1-2):181-6. doi: 10.1002/ajmg.1320430130.

Abstract

Since 1985, we have provided coordinated DNA-based and cytogenetic prenatal analysis for couples at risk for offspring afflicted with the fragile X [fra(X)] syndrome. To date, 40 pregnancies have been studied (22 males, 18 females). There were 5 males and 3 females identified to be at high risk by DNA but only 2 males and one female were demonstrated to be cytogenetically expressing the fra(X) prenatally. Of the other 3 males, one was a cytogenetic false negative (i.e. confirmed fra(X)+ at termination of pregnancy). The other 2 remain fra(X)- and are developing normally (undetected recombinants or non-penetrant male carriers). All fetuses at low risk were carried to term and are reported to be normal.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytogenetics / statistics & numerical data
  • DNA / genetics
  • DNA Probes
  • Diagnostic Errors
  • Female
  • Fragile X Syndrome / diagnosis*
  • Fragile X Syndrome / genetics
  • Gene Expression
  • Genetic Carrier Screening
  • Humans
  • Male
  • Pedigree
  • Pregnancy
  • Prenatal Diagnosis* / statistics & numerical data
  • Sensitivity and Specificity

Substances

  • DNA Probes
  • DNA