Evidence map›Paper›PMID 40114248›Full record

ArticleJournal of medical case reports2025

Kearns-Sayre syndrome presenting with progressive external ophthalmoplegia and third-degree atrioventricular block diagnostic challenge in resource-limited settings: a case report.

Gebeyehu Tessema Azibte, Zekarias Seifu Ayalew, Bereket Abraha Molla, Meseret Zewdie Ayele, Temesgen Baylie Bezabeh, Surafiel Adugna Wube, Biruk Abate Legesse, Tigist Kahsay Meresa

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Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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8 authors.

Gebeyehu Tessema AzibteCollege of Medicine and Health Sciences, Department of Internal Medicine, Addis Ababa University, Addis Ababa, Ethiopia. gebe10tessema@gmail.com.ORCID http://orcid.org/0009-0005-6849-1293
Zekarias Seifu AyalewCollege of Medicine and Health Sciences, Department of Internal Medicine, Addis Ababa University, Addis Ababa, Ethiopia.
Bereket Abraha MollaCollege of Medicine and Health Sciences, Department of Internal Medicine, Addis Ababa University, Addis Ababa, Ethiopia.
Meseret Zewdie AyeleCollege of Medicine and Health Sciences, Department of Neurology, Addis Ababa University, Addis Ababa, Ethiopia.
Temesgen Baylie BezabehCollege of Medicine and Health Sciences, Department of Neurology, Addis Ababa University, Addis Ababa, Ethiopia.
Surafiel Adugna WubeCollege of Medicine and Health Sciences, Department of Internal Medicine, Addis Ababa University, Addis Ababa, Ethiopia.
Biruk Abate LegesseCollege of Medicine and Health Sciences, Department of Internal Medicine, Addis Ababa University, Addis Ababa, Ethiopia.
Tigist Kahsay MeresaDepartment of Internal Medicine, Jimma University Medical Center, Jimma, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKearns-Sayre syndrome is a rare autosomal recessive mitochondrial disorder characterized by progressive external ophthalmoplegia and pigmentary retinopathy. Onset typically occurs before the age of 20 years and is attributed to mutations within mitochondrial DNA affecting proteins critical for the oxidative phosphorylation pathway. Since these mitochondrial disorders usually present with an isolated manifestation such as complete heart block, a meticulous search for other organ-specific manifestations is necessary for an early diagnosis. Reporting such cases facilitates recognition of common clinical presentations, enabling earlier diagnosis, earlier interventions, and genetic counseling. CASE PRESENTATION: A 29-year-old right-handed Ethiopian male patient presented with progressive exercise intolerance for 10 years. He had had bilateral ptosis since childhood and experienced gait difficulty with intermittent balance problems, particularly at night. In 2018, he was diagnosed with a third-degree atrioventricular block with a resting electrocardiogram, and a permanent pacemaker was placed. Despite marked improvement in shortness of breath following pacemaker placement, the patient's progressive ptosis and gait ataxia prompted further workup, ultimately leading to the diagnosis of Kearns-Sayre syndrome. This case highlights the importance of comprehensive assessment in patients presenting with isolated organ manifestations, as exemplified by the delayed diagnosis of Kearns-Sayre syndrome following the initial recognition of a complete heart block.

conclusionGiven the early-onset nature of Kearns-Sayre syndrome, it should be considered as a differential diagnosis in young individuals presenting with complete heart block. A thorough evaluation for additional organ involvement is crucial in such cases, as early intervention and genetic counseling significantly impact patient outcomes.

Indexed as

Atrioventricular BlockKearns-Sayre SyndromeAdultBlepharoptosisDiagnosis, DifferentialElectrocardiographyGait AtaxiaHumansMalePacemaker, ArtificialResource-Limited SettingsComplete heart blockKearns–Sayre syndromeMitochondrial disorderPigmentary retinopathyProgressive external ophthalmoplegia

Identifiers

PMID40114248
PMCPMC11924816

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