Kearns-Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathy

Neurology. 1993 Jan;43(1):218-21. doi: 10.1212/wnl.43.1_part_1.218.

Abstract

Mitochondrial DNA (mtDNA) was deleted in a patient with Kearns-Sayre syndrome (KSS) presenting with a choroideremia-like fundus picture instead of pigmentary retinopathy. No evidence for X-linked choroideremia was present, and because of the strong association between KSS and deleted mtDNA, we suggest that choroideremia is a phenocopy and can be part of KSS.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Choroideremia / genetics*
  • DNA, Mitochondrial / analysis*
  • Humans
  • Karyotyping
  • Kearns-Sayre Syndrome / genetics*
  • Male
  • Sequence Deletion*

Substances

  • DNA, Mitochondrial