Abstract
Kearns-Sayre syndrome (KSS) is a rare mitochondrial disorder with a triad of progressive external ophthalmoplegia, pigmentary retinopathy with onset before age 20. KSS is associated with unpredictably progressive conduction system abnormalities which mandates regular follow-ups. 28-year-old male
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
