, Additionally, some inconsistencies require clarification

M. Leal, C. Dhoble, J. Lee, D. Lopez, and L. S. Menéndez, 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, vol.2016, pp.34-40, 2016.

E. Wilichowski, G. C. Korenke, W. Ruitenbeek, D. Meirleir, L. Hagendorff et al., Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutation, J Neurol Sci, vol.157, pp.206-219, 1998.

S. Seneca, H. Verhelst, D. Meirleir, L. Meire, F. Ceuterick-de-groote et al., A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome, Arch Neurol, vol.58, pp.1113-1121, 2001.

|. J. Finsterer and S. Zarrouk-mahjoub,