ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy

Kathleen M. Fitzgerald, Gerhard W. Cibis, Ann Headrick Gettel, Robert Rinaldi, David J. Harris, Robert A. White

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Purpose - Mutations in the dystrophin gene result in Duchenne muscular dystrophy (DMD). DMD is associated with an abnormal electroretinogram (ERG) if the mutation disrupts the translation of retinal dystrophin (Dp260). Our aim was to determine if incomplete ERG abnormalities would be associated with heterozygous carriers of dystrophin gene mutations. Methods - Ganzfeld ERGs were obtained under scotopic and photopic testing conditions from a family which includes the heterozygous maternal grandmother, the heterozygous mother, and her children, two affected boys and dizygotic twin sibs, an unaffected male and heterozygous female. Southern blot analyses were done to characterise the dystrophin mutation. Results - The dystrophin gene was found to contain a deletion encompassing exon 50. The ERGs in the two affected boys were abnormal, consistent with the DMD ERG phenotype. Serial ERGs of the heterozygous females were abnormal; however, they were less severely affected than the DMD boys. The ERG of the female sib showed a greater abnormality than her mother and maternal grandmother. The unaffected twin had a normal ERG. Conclusions - The ERG shows abnormalities associated with carrier status in this family with a single exon deletion. A large study of confirmed obligate carriers is planned to clarify further the value of the ERG in detecting female heterozygous carriers of dystrophy gene mutations.

Original languageEnglish (US)
Pages (from-to)316-322
Number of pages7
JournalJournal of Medical Genetics
Volume36
Issue number4
StatePublished - Jan 1 1999

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Dystrophin
Duchenne Muscular Dystrophy
Phenotype
Mutation
Mothers
Genes
Exons
Dizygotic Twins
Southern Blotting

Keywords

  • Dystrophin
  • Electroretinography
  • Muscular dystrophy
  • Retina

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Fitzgerald, K. M., Cibis, G. W., Gettel, A. H., Rinaldi, R., Harris, D. J., & White, R. A. (1999). ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy. Journal of Medical Genetics, 36(4), 316-322.

ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy. / Fitzgerald, Kathleen M.; Cibis, Gerhard W.; Gettel, Ann Headrick; Rinaldi, Robert; Harris, David J.; White, Robert A.

In: Journal of Medical Genetics, Vol. 36, No. 4, 01.01.1999, p. 316-322.

Research output: Contribution to journalArticle

Fitzgerald, KM, Cibis, GW, Gettel, AH, Rinaldi, R, Harris, DJ & White, RA 1999, 'ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy', Journal of Medical Genetics, vol. 36, no. 4, pp. 316-322.
Fitzgerald, Kathleen M. ; Cibis, Gerhard W. ; Gettel, Ann Headrick ; Rinaldi, Robert ; Harris, David J. ; White, Robert A. / ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy. In: Journal of Medical Genetics. 1999 ; Vol. 36, No. 4. pp. 316-322.
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