Ophthalmoplegia, pigmentary retinopathy, and abnormal cardiac conduction: A rare case of Kearns-Sayre syndrome

Ophthalmoplegia, pigmentary retinopathy, and abnormal cardiac conduction: A rare case of Kearns-Sayre syndrome

Kearns-Sayre syndrome (KSS) is one of the three classic and overlapping phenotypes that result from simplex mitochondrial DNA (mtDNA) deletion syndromes. The rarity of the syndrome has led to a paucity of reported cases in the literature. We present the case of a young female who presented with droo...

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Bibliographic Details
Main Authors: Arsalan Nadeem, Sumayya Umar, Sohaib Rehmani, Mustafa Javaid
Format: Article
Language:English
Published: Elsevier 2023-03-01
Series:eNeurologicalSci
Subjects:
Myopathy
Mitochondrial DNA
Ophthalmoplegia
Retinopathy
Infarct
Extraocular
Online Access:http://www.sciencedirect.com/science/article/pii/S2405650223000060

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http://www.sciencedirect.com/science/article/pii/S2405650223000060

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