Kearns-Sayre syndrome

نویسنده

  • K S CHANNER
چکیده

The Kearns-Sayre syndrome is a mitochondrial myopathy characterised by ptosis, chronic progressive external ophthalmoplegia, abnormal retinal pigmentation, and cardiac conduction defects. A unique case is reported in which there was rapid development ofprogressive congestive cardiac failure that required cardiac transplantation. A review of published reports of mitochondrial myopathy shows that a minority of cases (< 20%) have cardiac involvement. This had previously been limited to abnormalities of cardiac conduction with progressive heart block. Myocardial biopsy has, however, shown ultrastructural evidence of a generalised mitochondrial disorder which hitherto has not been associated with a functional deficit.

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Hypoparathyroidism as the First Mani-Festation of Kearns-Sayre Syndrome: A Case Report

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Kearns-Sayre syndrome--a case report.

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A novel mitochondrial DNA deletion in a Chinese girl with Kearns-Sayre syndrome.

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[PCR-based detection of heteroplasmic deleted mitochondrial DNA in Kearns-Sayre syndrome].

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[Cardiac involvement in Kearns-Sayre syndrome].

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تاریخ انتشار 2005