Literature DB >> 21165624

[Kearns-Sayre syndrome : a mitochondrial disease (OMIM #530000)].

W J Mayer1, M Remy, G Rudolph.   

Abstract

Kearns-Sayre syndrome is a rare mitochondrial disease which usually occurs sporadically with the presence of ptosis and the clinical triad of chronic progressive external ophthalmoplegia, atypical retinitis pigmentosa and cardiac conduction disorders. We show on the example of a young patient with unexplained atypical acquired ptosis and eye movement disorders, the correct interpretation of the diagnostic findings. Of importance is the early detection of potentially life-threatening complications which can lead to sudden cardiac death.

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Year:  2011        PMID: 21165624     DOI: 10.1007/s00347-010-2296-3

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN: 0941-293X            Impact factor:   1.059


  16 in total

1.  Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases.

Authors:  T P KEARNS; G P SAYRE
Journal:  AMA Arch Ophthalmol       Date:  1958-08

Review 2.  The diagnosis of mitochondrial muscle disease.

Authors:  Robert W Taylor; Andrew M Schaefer; Martin J Barron; Robert McFarland; Douglass M Turnbull
Journal:  Neuromuscul Disord       Date:  2004-04       Impact factor: 4.296

3.  Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation.

Authors:  Johannes A Mayr; Olaf Merkel; Sepp D Kohlwein; Boris R Gebhardt; Hansjosef Böhles; Ulrike Fötschl; Johannes Koch; Michaela Jaksch; Hanns Lochmüller; Rita Horváth; Peter Freisinger; Wolfgang Sperl
Journal:  Am J Hum Genet       Date:  2007-01-10       Impact factor: 11.025

4.  Genotyping in urine: an interesting tool for epidemiological studies.

Authors:  V Haufroid; A Clippe; B Knoops; A Bernard; D Lison
Journal:  Clin Chem       Date:  1998-10       Impact factor: 8.327

5.  Kearns-Sayre syndrome: cerebral folate deficiency, MRI findings and new cerebrospinal fluid biochemical features.

Authors:  Mercedes Serrano; María Teresa García-Silva; Elena Martin-Hernandez; Maria del Mar O'Callaghan; Pilar Quijada; Ana Martinez-Aragón; Aida Ormazábal; Alberto Blázquez; Miguel A Martín; Paz Briones; Ester López-Gallardo; Eduardo Ruiz-Pesini; Julio Montoya; Rafael Artuch; Mercedes Pineda
Journal:  Mitochondrion       Date:  2010-04-11       Impact factor: 4.160

6.  Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia.

Authors:  D A Drachman
Journal:  Arch Neurol       Date:  1968-06

7.  Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin.

Authors:  Dirk Lebrecht; Aikaterini Kokkori; Uwe-Peter Ketelsen; Bernhard Setzer; Ulrich A Walker
Journal:  J Pathol       Date:  2005-12       Impact factor: 7.996

8.  Improved brain and muscle mitochondrial respiration with CoQ. An in vivo study by 31P-MR spectroscopy in patients with mitochondrial cytopathies.

Authors:  B Barbiroli; S Iotti; R Lodi
Journal:  Biofactors       Date:  1999       Impact factor: 6.113

Review 9.  Neuro-ophthalmology of mitochondrial diseases.

Authors:  Valérie Biousse; Nancy J Newman
Journal:  Curr Opin Neurol       Date:  2003-02       Impact factor: 5.710

10.  [Chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome : interdisciplinary diagnosis and therapy].

Authors:  B Wabbels; N Ali; W S Kunz; P Roggenkämper; C Kornblum
Journal:  Ophthalmologe       Date:  2008-06       Impact factor: 1.059

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