A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles

Research output: Contribution to journalArticle

Abstract

Kearns-Sayre syndrome is a mitochondrial disorder characterized by the emergence before the age of 20 years of progressive external ophthalmoplegia, pigmentary retinopathy, with other heterogeneous clinical manifestations. Generally, mitochondrial DNA deletions were associated with KSS but the size and position of these deletions differ among patients. This study reported a Tunisian patient with typical features of KSS. Long-range PCR amplification of the mtDNA in different tissues from this patient showed multiple mitochondrial deletions: two novel 9.768 and 7.253 kb deletions spanning respectively nucleotides 6124-15,893 and 8572-15,826 associated with the common 4.977 kb deletion.

Details

Authors
  • Emna Mkaouar-Rebai
  • Imen Chamkha
  • Thouraya Kammoun
  • Imen Chabchoub
  • Hajer Aloulou
  • Nourhene Fendri
  • Mongia Hachicha
  • Faiza Fakhfakh
External organisations
  • University of Sfax
Research areas and keywords

Keywords

  • Adolescent, Brain, DNA, Mitochondrial, Female, Hair Follicle, Humans, Kearns-Sayre Syndrome, Leukocytes, Magnetic Resonance Imaging, Mouth Mucosa, Sequence Deletion, Tunisia
Original languageEnglish
Pages (from-to)449-55
Number of pages7
JournalMitochondrion
Volume10
Issue number5
Publication statusPublished - 2010 Aug
Publication categoryResearch
Peer-reviewedYes
Externally publishedYes