Kearns syndrome or Kearns disease. Further evidence of a genuine entity in a case with uncommon features

Ophthalmologica. 1982;184(1):40-50. doi: 10.1159/000309183.

Abstract

A 20-year-old man with the characteristic findings of infantile onset Kearns syndrome is described. Morphological and biochemical investigations proved a mitochondrial disease which we believe to be the cause of the symptoms in various organs. We assume an autosomal-dominant inheritance, the marker sign of which is blepharoptosis in several family members. Characteristic clinical, morphological and biochemical findings, combined with an autosomal-dominant inheritance with very variable expression, mark the Kearns syndrome as an individual disease, not as a symptom complex (syndrome). Kearns disease can be divided into three forms--an infantile form ("Kearns-Sayre syndrome') with early onset, rapid progression, multisystemic involvement and a severe course; and a juvenile and an adult form with onset in the second, respectively third (or later) decades with a generally slower and more benign course and less widespread expression in various organ systems. Furthermore, the occurrence of a curious orthoptic abnormality is described, indicating one of the possible ways to avoid diplopia in chronic progressive external ophthalmoplegia: the coexistence of normal and gliding abnormal retinal correspondence.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Blepharoptosis / complications
  • Blepharoptosis / genetics*
  • Child
  • Child, Preschool
  • Eye Diseases / diagnosis
  • Female
  • Fixation, Ocular
  • Fluorescein Angiography
  • Genes, Dominant
  • Humans
  • Male
  • Microscopy, Electron
  • Mitochondria, Muscle / ultrastructure
  • Ophthalmoplegia / complications*
  • Pedigree
  • Pigment Epithelium of Eye*
  • Syndrome