van BeynumI., MoravaE., TaherM., et al. (2012). Cardiac arrest in Kearns-Sayre syndrome. JIMD Rep, 2, 7–10.
2.
ChuB.C., TeraeS., TakahashiC., et al. (1999). MRI of the brain in the Kearns-Sayre syndrome: report of four cases and a review. Neuroradiology, 41, 759–764.
3.
FinstererJ., and FrankM. (2016). Prevalence of neoplasms in definite and probable mitochondrial disorders. Mitochondrion, 29, 31–34.
4.
GuoL., WangX., JiH. (2020). Clinical phenotype and genetic features of a pair of Chinese twins with Kearns-Sayre syndrome. DNA Cell Biol, 39, 1449–1457.
5.
KabungaP., LauA.K., PhanK. et al. (2015). Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathy. Int J Cardiol, 181, 303–310.
6.
KangY.X., WangY.J., ZhangQ., PangX.H., and GuW. (2017). A case of hypopituitarism accompanying Kearns-Sayre syndrome treated with human chorionic gonadotropin: a case report and literature review. Andrologia 49,e12711.
7.
SehgalS., ChoudhryS., DebelenkoL., and L'EcuyerT. (2016). Dilated cardiomyopathy with cardiogenic shock in a child with Kearns-Sayre syndrome. BMJ Case Rep, 2016, DOI: 10.1136/bcr-2015-213813
8.
ShemeshA., and MargolinE. (2020). Kearns Sayre syndrome. In: StatPearls. (StatPearls Publishing, Treasure, Island, FL).