[Pattern dystrophies and intrafamilial phenotypic variation]

Klin Monbl Augenheilkd. 1996 May;208(5):291-3. doi: 10.1055/s-2008-1035218.
[Article in French]

Abstract

Background: Transmitted in an autosomal dominant fashion, the pattern dystrophies involve the retinal pigment epithelium and the external macular retina and are usually divided into four different entities. However, a progression from one form to another is possible, various forms may coexist in the same patient and a combination of different entities may be present in the same family.

Case reports: Two families (4 cases) are described, in which a butterfly dystrophy coexist with a vitelliform dystrophy or with a central atrophy. Whereas the vitelliform dystrophy is usually characterised by a unique centromacular lesion, a case of multiple lesions is described. The possible association with a neovascular membrane is also presented.

Conclusion: The coexistence of various forms of pattern dystrophies in a same family suggests a variable expression of a same genetic disorder. The presence of a centromacular atrophy in one patient demonstrates also that the spectrum of the disease is not limited to the four classic entities.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adult
  • Aged
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Corneal Dystrophies, Hereditary / classification
  • Corneal Dystrophies, Hereditary / diagnosis
  • Corneal Dystrophies, Hereditary / genetics*
  • Diagnosis, Differential
  • Fluorescein Angiography
  • Genes, Dominant / genetics*
  • Humans
  • Macula Lutea / pathology
  • Male
  • Phenotype
  • Pigment Epithelium of Eye / pathology
  • Retinal Degeneration / classification
  • Retinal Degeneration / diagnosis
  • Retinal Degeneration / genetics*
  • Retinal Neovascularization / classification
  • Retinal Neovascularization / diagnosis
  • Retinal Neovascularization / genetics
  • Vitreoretinopathy, Proliferative / classification
  • Vitreoretinopathy, Proliferative / diagnosis
  • Vitreoretinopathy, Proliferative / genetics