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

Abstract Background Kearns–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 protein...

وصف كامل

التفاصيل البيبلوغرافية

المؤلفون الرئيسيون:	Gebeyehu Tessema Azibte, Zekarias Seifu Ayalew, Bereket Abraha Molla, Meseret Zewdie Ayele, Temesgen Baylie Bezabeh, Surafiel Adugna Wube, Biruk Abate Legesse, Tigist Kahsay Meresa
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	BMC 2025-03-01
سلاسل:	Journal of Medical Case Reports
الموضوعات:	Kearns–Sayre syndrome Mitochondrial disorder Complete heart block Progressive external ophthalmoplegia Pigmentary retinopathy
الوصول للمادة أونلاين:	https://doi.org/10.1186/s13256-025-05086-5
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!