Lone noncompaction in Leber's hereditary optic neuropathy

Acta Cardiologica

Volumn 59, Issue 2, 2004, Pages 187-190

  Finsterer, Josef ^a,b   Stöllberger, Claudia ^a   Prainer, Christian ^a   Hochwarter, Anelia ^a  

^a KRANKENANSTALT RUDOLFSTIFTUNG   (Austria)

^b NONE   (Austria)

Author keywords

Encephalomyopathy; Hypertrabeculation; Mitochondrial; Neuromuscular disorder; Optic atrophy; Respiratory chain

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CENTRAL SCOTOMA; CLINICAL FEATURE; CONGENITAL HEART DISEASE; DISEASE ASSOCIATION; EVOKED VISUAL RESPONSE; HEART LEFT VENTRICLE NONCOMPACTION; HUMAN; HYPEREMIA; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; TELANGIECTASIA; TRANSTHORACIC ECHOCARDIOGRAPHY; VISUAL ACUITY; VISUAL FIELD DEFECT; VISUAL IMPAIRMENT;

ADULT; ECHOCARDIOGRAPHY; HEART DEFECTS, CONGENITAL; HUMANS; MALE; OPTIC ATROPHY, HEREDITARY, LEBER;

EID: 1942440371     PISSN: 00015385     EISSN: None     Source Type: Journal    
DOI: 10.2143/AC.59.2.2005175     Document Type: Article

References (10)

1. Stöllberger C, Finsterer J, Blazek G. Left ventricular hypertrabeculation/noncompaction and association with additional cardiac abnormalities and neuromuscular disorders. Am J Cardiol 2002; 90: 899-902.
2. Stöllberger C, Finsterer J, Blazek G. Isolated left ventricular abnormal trabeculation: Follow-up and association with neuromuscular disorders. Can J Cardiol 2001; 17: 163-8.
3. Finsterer J, Stöllberger C, Michaela J. Familial left ventricular hypertrabeculation in two blind brothers. Cardiovasc Pathol 2002; 11: 146-8.
4. Oechslin EN, Attenhofer Jost CH, Rojas JR, Kaufmann PA, Jenni, R. Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis. J Am Coll Cardiol 2000; 36: 493-500.
5. Hamamichi Y, Ichida F, Hashimoto I, Hirono K, Uese K, Miyawaki T, Tsukano S, Ono Y, Echigo S, Kamiya T. Isolated noncompaction of the ventricular myocardium: Ultra fast computed tomography and magnetic resonance imaging. Int J Card Imaging 2001; 17: 305-14.
6. Finsterer J, Stöllberger C, T, Feichtinger H. Non-compaction on echocardiography and autopsy. Acta Cardiol 2003; 58: 165-8.
7. Ichida F, Hamamichi Y, Miyawaki T, Ono Y, Kamiya T, Akagi T, Hamada H, Hirose O, Isobe T, Yamada K, Kurotobi S, Mito H, Miyake T, Murakami Y, Nishi T, Shinohara M, Seguchi M, Tashiro S, Tomimatsu H. Clinical features of isolated noncompaction of the ventricular myocardium. Long-term clinical course, hemodynamic properties, and genetic background. J Am Coll Cardiol 1999; 34: 233-40.
8. Riordan-Eva P, Sanders M, Govan GG, Sweeney MG, DaCosta J, Harding AE. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 1995; 118: 319-37.
9. Matsumoto M, Hayasaka S, Kadoi C, Hotta V, Fujiki K, Takeda M, Ishida N, Endo S, Kanai A. Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy. Ophthalmic Genet 1999; 20: 153-60.
10. Nikòskelainen EK, Savontaus M-L, Huoponen K, Antila K, Hartiale J. Pre-excitation syndrome in Leber's hereditary optic neuropathy. Lancet 1994; 344: 857-8.