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Kearns–Sayre syndrome: a case series of 35 adults and children

Authors Khambatta S, Nguyen DL, Beckman TJ, Wittich CM

Received 5 April 2014

Accepted for publication 29 April 2014

Published 3 July 2014 Volume 2014:7 Pages 325—332

DOI https://doi.org/10.2147/IJGM.S65560

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3

Sherezade Khambatta, Douglas L Nguyen, Thomas J Beckman, Christopher M Wittich

Division of General Internal Medicine, Mayo Clinic, Rochester, MN, USA

Background: Kearns–Sayre syndrome (KSS) is a rare mitochondrial cytopathy, first described at Mayo Clinic in 1958.
Aims: We aimed to define patient and disease characteristics in a large group of adult and pediatric patients with KSS.
Methods: We retrospectively searched the Mayo Clinic medical index patient database for the records of patients with KSS between 1976 and 2009. The 35 patients identified with KSS were analyzed in terms of demographic characteristics, presenting signs and symptoms, diagnostic features, clinical evolution, and associations between disease features and the development of disability.
Results: The mean (standard [SD]) age at KSS presentation was 17 (10) years, but the mean age at diagnosis was 26 (15) years. Ophthalmologic symptoms developed in all patients, and neurologic and cardiac involvement was common. Only four patients (11%) in the series died, but all deaths were from sudden cardiac events. The development of physical disability was significantly associated with cognitive decline (P=0.004) but not with other clinical features, such as sex or sudden cardiac death.
Conclusion: We report the largest case series to date of patients with KSS from a single institution. In addition to the conduction system abnormalities identified in previous series, our cohort included patients with syncope and sudden cardiac death. This underscores the need to consider formal electrophysiologic studies and prophylactic defibrillators in patients with KSS.

Keywords: heart block, mitochondrial diseases, ophthalmoplegia, retinitis pigmentosa

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