Segregation of the fragile X mutation from an affected male to his normal daughter

Hum Mol Genet. 1992 Oct;1(7):511-5. doi: 10.1093/hmg/1.7.511.

Abstract

We report here a family in which the fragile X mutation segregates from an affected grandfather through his normal daughter to an affected grandson. The grandson shows clinical and cytogenetic expression of fragile X syndrome due to a full mutation (large methylated insertion) in the fragile X gene (FMR-1). The mother shows a premutation (small unmethylated insertion) in her FMR-1 gene as the sole manifestation of the fragile X syndrome. The grandfather expresses the fragile X syndrome at the clinical and cytogenetic level, whereas he is mosaic for a methylated full mutation and an unmethylated premutation. The absence of expression of the fragile X mutation when transmitted through an expressing male might present further evidence for genomic imprinting of the FMR-1 gene. Alternatively, it is possible that the grandfather transmitted his premutation to his daughter due to germline mosaicism with both the premutation and the full mutation present in his sperm.

Publication types

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

MeSH terms

  • Adult
  • Arylsulfatases / blood
  • Child, Preschool
  • Female
  • Fragile X Syndrome / genetics*
  • Humans
  • Ichthyosis, X-Linked / genetics
  • Leukocytes / enzymology
  • Male
  • Middle Aged
  • Mutation*
  • Pedigree
  • Steryl-Sulfatase

Substances

  • Arylsulfatases
  • Steryl-Sulfatase