Open AccessDiagnose Kearns–Sayre syndrome genetically and investigate the phenotype comprehensively
Author(s) -
Josef Finsterer,
Sinda ZarroukMahjoub
Publication year - 2016
Publication title -
oxford medical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.169
H-Index - 9
ISSN - 2053-8855
DOI - 10.1093/omcr/omw059
Subject(s) - medicine , ptosis , kearns–sayre syndrome , presentation (obstetrics) , phenotype , genetics , surgery , biology , gene , mitochondrial dna
Letter to the editor Comment on : Leal M Dhoble C Lee J Lopez D Menendez LS . A rare case of Kearns-Sayre syndrome in a 17-year-old Venezuelan male with bilateral ptosis as the initial presentation. Oxf Med Case Reports 2016;2016:34–6.
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