Cardiac abnormalities in patients with Leber's hereditary optic neuropathy

Heart

Volumn 89, Issue 7, 2003, Pages 791-792

  Sorajja, P ^a,c   Sweeney, M G ^b   Chalmers, R ^b   Sachdev, B ^a   Syrris, P ^a   Hanna, M ^b   Wood, N D ^b   McKenna, W J ^a   Elliott, P M ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^b NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^c MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; ECHOCARDIOGRAPHY; FEMALE; HEART DISEASE; HEART FUNCTION; HEART LEFT ATRIUM; HEART LEFT VENTRICLE HYPERTROPHY; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; MORPHOLOGY; PREVALENCE; PRIORITY JOURNAL; PROVOCATION TEST; ST SEGMENT; T WAVE;

EID: 0038545847     PISSN: 13556037     EISSN: None     Source Type: Journal    
DOI: 10.1136/heart.89.7.791     Document Type: Article

References (5)

1. Newman NJ. Leber's hereditary optic neuropathy. Ophthalmol Clin North Am 1991;4:431.
2. Wallace DC, Lott, Brown MD, et al. Report of the committee on human mitochondrial DNA. In: Cuticchia AJ, Pearson PL, eds. Human gene mapping: a compendium. Baltimore: Johns Hopkins University Press; 1995:910-54.
3. Nikoskelainen E, Wanne O, Dahl M. Pre-excitatlon syndrome and Leber's hereditary optic neuroretinopathy. Lancet 1985;i:696.
4. Eva-Riordan P, Harding AE. Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. J Med Genet 1995;32:81-7.
5. Bower SPC, Hawley I, Mackey DA. Cardiac arrhythmia and Leber's hereditary optic neuropathy. Lancet 1992;339:1427-8.