Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA

Am J Med Genet. 1991 Mar 15;38(4):616-21. doi: 10.1002/ajmg.1320380423.

Abstract

We report carrier identification and a prenatal diagnosis using DNA polymorphisms in 2 families with X-linked Pelizaeus-Merzbacher disease (PMD). In both families, the proteolipid protein (PLP) gene in the single affected male could be traced back to his unaffected maternal grandfather. Therefore, each family contains a new mutation. In the case of the prenatal diagnosis, the fetus was shown by cytogenetic analysis to be a female, who we predict will be a noncarrier of PMD based on her genotype with the PLP intragenic polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA / analysis
  • Diffuse Cerebral Sclerosis of Schilder / diagnosis*
  • Diffuse Cerebral Sclerosis of Schilder / genetics
  • Female
  • Genetic Carrier Screening*
  • Genetic Linkage
  • Humans
  • Male
  • Pedigree
  • Polymorphism, Restriction Fragment Length
  • Prenatal Diagnosis
  • Proteolipids / genetics*

Substances

  • Proteolipids
  • DNA