Literature DB >> 6627817

Near-fatal Kearns-Sayre syndrome. A case report and review of clinical manifestations.

K S Rheuban, N A Ayres, T D Sellers, J P DiMarco.   

Abstract

The Kearns-Sayre syndrome is a relatively uncommon condition which occurs in childhood and is characterized by neurologic dysfunction and abnormalities in atrioventricular (AV) conduction. The high mortality rate is directly attributable to the cardiovascular manifestations of this syndrome. We report a case, with documentation of a "near-fatal" episode, and review the pertinent clinical features of the syndrome.

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Year:  1983        PMID: 6627817     DOI: 10.1177/000992288302201208

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  3 in total

1.  Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome.

Authors:  P Runge; D Calver; J Marshall; D Taylor
Journal:  Br J Ophthalmol       Date:  1986-10       Impact factor: 4.638

Review 2.  Mitochondrial DNA mutations in renal disease: an overview.

Authors:  Larissa P Govers; Hakan R Toka; Ali Hariri; Stephen B Walsh; Detlef Bockenhauer
Journal:  Pediatr Nephrol       Date:  2020-01-10       Impact factor: 3.714

3.  Combined occurrence of diabetes mellitus and retinitis pigmentosa.

Authors:  Afaf Al-Adsani; Fadl Abdel Gader
Journal:  Ann Saudi Med       Date:  2010 Jan-Feb       Impact factor: 1.526

  3 in total

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