[Changing perception of hereditary eye diseases]

Ned Tijdschr Geneeskd. 2002 Feb 23;146(8):345-50.
[Article in Dutch]

Abstract

The authors present the cases of two parents with Usher syndrome type I who appeared to have normal offspring, and two families, one with autosomal dominant retinoblastoma and a RB1-gene mutation and one with primary open angle glaucoma and a myocilin gene mutation, in whom DNA-analysis was used to see whether check-ups were needed. The field of ophthalmogenetics comprises many disorders, both congenital and those with a later onset. Mendelian, mitochondrial, as well as multifactorial heredity is seen. Recent progress in this field, especially in molecular genetics, has created new possibilities, but some situations appear to be more complex than previously assumed. Particularly if there is genetic heterogeneity or multifactorial inheritance, possibilities for counselling and DNA analysis remain limited.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • Eye Diseases, Hereditary / diagnosis
  • Eye Diseases, Hereditary / genetics*
  • Eye Proteins / genetics*
  • Female
  • Genetic Linkage
  • Glaucoma, Open-Angle / diagnosis
  • Glaucoma, Open-Angle / genetics*
  • Humans
  • Infant
  • Male
  • Mutation
  • Pedigree
  • Retinal Neoplasms / diagnosis
  • Retinal Neoplasms / genetics
  • Retinoblastoma / diagnosis
  • Retinoblastoma / genetics
  • Retinoblastoma Protein / genetics
  • Syndrome
  • Trabecular Meshwork

Substances

  • Eye Proteins
  • Retinoblastoma Protein