Subacute necrotising encephalopathy in an Alaskan husky

Journal of Small Animal Practice

Volumn 40, Issue 12, 1999, Pages 585-589

  Wakshlag, J J ^a   De Lahunta, A ^a   Robinson, T ^b   Cooper, B J ^a   Brenner, O ^a   O'Toole, T D ^c   Olson, J ^d   Beckman, K B ^e   Glass, E ^f   Reynolds, A J ^a  

^a Department of Obstetrics Gynecology   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c UNIVERSITY OF WYOMING   (United States)

^d Raven Veterinary Services   (United States)

^e UNIVERSITY OF ALASKA FAIRBANKS   (United States)

^f UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ANIMAL DISEASE; ARTICLE; CASE REPORT; CEREBELLUM CORTEX; DISEASE COURSE; DOG; DOG DISEASE; FEMALE; LEIGH DISEASE; MITOCHONDRIAL ENCEPHALOMYOPATHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY;

ANIMALS; CEREBELLAR CORTEX; DISEASE PROGRESSION; DOG DISEASES; DOGS; FEMALE; LEIGH DISEASE; MAGNETIC RESONANCE IMAGING; MITOCHONDRIAL ENCEPHALOMYOPATHIES;

EID: 0033252463     PISSN: 00224510     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1748-5827.1999.tb03028.x     Document Type: Article

References (31)

1. ADAMS, P. L. & TURNBULL, D. M. (1996) Disorders of the respiratory chain. Journal of Inherited and Metabolic Disorders 19, 463-469
2. BRENNER, O., DE LAHUNTA, A., SUMMERS, B. A., CUMMINGS, J. F., COOPER, B. J., VALENTINE, B. A. & BELL, J. S. (1997a) Hereditary polioencephalomyelopathy of the Australian cattle dog. Acta Neuropathologica 94, 54-66
3. BRENNER, O., DE LAHUNTA, A., SUMMERS, B. A., CUMMINGS, J. F. & MONACHELLI, M. (1997b) A canine encephalomyelopathy with morphological abnormalities in mitochondria. Acta Neuropathotogica 94, 390-397
4. CALVANI, A., KOVERECH, A. & CARUSO, G. (1993) Treatment of mitochondrial disorders. In: Mitochondrial DNA in Human Pathology. Eds S. DiMauro and D. C. Wallace. Raven Press, New York. pp 173-199
5. DEGOUL, F., DIRY, M., RODRIGUEZ, D., ROBAIN, O., FRANCOIS, D., PONSOT, G., MARSAC, C. & DESGUERRE, G. (1995) Clinical, biochemical and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the T8993G point mutation. Journal of Inherited Metabolic Diseases 20, 49-52
6. DEGOUL, F., FRANCOIS, D., DIRY, M., PONSOT, G., DESGUERRE, I., HERON, B., MARSAC, C. & MOUTARD, M. L. (1997) A near homoplasmic T3993G mtDNA mutation in a patient with atypic Leigh Syndrome not present in the mother's tissues. Journal of Inherited and Metabolic Disorders 20, 49-53
7. DIMAURO, S. (1996) Mitochondrial encephalomyopathies: what next? Journal of Inherited and Metabolic Disorders 19, 489-503
8. DIMAURO, S. & DEVIVO, D. C. (1996) Genetic heterogeneity in Leigh syndrome. Annals of Neurology 40, 5-7
9. DIMAURO, S. & MORAES, C. T. (1993) Mitochondrial encephalomyopathies. Archives of Neurology 50, 1197-1208
10. DIMAURO, S., SERVIDEI, S., ZEVIANI, M., DIROCCA, M., DEVIVO, D. C., DIDONATO, S., UZIEL, G., BERRY, K., HOGANSON, G., JOHNSEN, S. D. & JOHNSON, P. C. (1987) Cytochrome c oxidase deficiency in Leigh Syndrome. Annals of Neurology 22, 498-506
11. GREENHOUSE, A. H. & SCHNECK, S. A. (1968) Subacute necrotizing encephalomyelopathy. Neurology 18, 1-8
12. HARDMAN, J. M., ALLEN, L. W., BAUGHMAN, F. A. & WATERMAN, D. F. (1968) Subacute necrotizing encephalopathy in late adolescence. Archives of Neurology 18, 478-486
13. JACKSON, M. J., SCHAEFER, J. A., JOHNSON, M. A., MORRIS, A. A. M., TURNBULL, D. M. & BINDOFF, L. A. (1995) Presentation and clinical investigation of mitochondrial respiratory chain disease. Brain 118, 339-357
14. JOHNS, D. R. (1995) Mitochondrial DNA and disease. New England Journal of Medicine 333, 638-644
15. LEWIS, A. J. (1965) Infantile subacute necrotizing encephalopathy. Canadian Medical Association Journal 93, 878-881
16. LIGHTOWLERS, R. N., CHINNERY, P. F., TURNBULL, D. M. & HOWELL, N. (1997) Mammalian mitochondrial genetics: heredity, heteroplasmy and disease. Trends in Genetics 13, 450-455
17. MORRIS, A. A. M., LEONARD, J. V., BROWN, G. K., BIDOUKI, S. K., BINDOFF, L. A., WOODWARD, C. C., HARDING, A. E., LAKE, B. D., HARDING, B. N., FARRELL, C. E., BELL, J. E., MIRAKHUR, M. & TURNBULL, D. M. (1996) Deficiency of respiratory chain complex I is a common cause of Leigh disease. Annals of Neurology 40, 25-30
18. OLBY, N. J., SCHOLES, S. F. E., JEFFREY, M., HANNAM, D. A. R. & BLAKEMORE, W. F. (1997) Characterization of a new encephalopathy in Swaledale lambs. Proceedings of the American College of Veterinary Internal Medicine, June. p 63
19. POGGI-TRAVERT, F., MARTIN, D., BILLETTE DE VILLEMEUR, T., BONNEFONT, J. P., VASSAULT, A., RABIER, D., CHARPENTIER, C., KAMOUN, P., MUNNICH, A. & SAUDUBRAY, J. M. (1996) Metabolic intermediates in lactic acidosis: compounds, samples, and interpretation. Journal of Inherited Metabolic Diseases 19, 478-488
20. RAHMAN, S., BLOK, R. B., DAHL, H. H., DANKS, D. M., KIRBY, D. M., CHOW, C. W., CHRISTODOULOU, J. & THORBURN, D. R. (1996) Leigh syndrome: clinical features and biochemical abnormalities. Annals of Neurology 39, 343-351
21. RICHTER, R. B. (1968) Infantile subacute necrotizing encephalopathy (Leigh's disease). Neurology 18, 1125-1132
22. ROBINSON, B. H., MACKAY, N., CHUN, K. & LING, M. (1996) Disorders of pyruvate and the pyruvate dehydrogenase complex. Journal of Inherited Metabolic Diseases 19, 452-462
23. SPARACO, M., BONILLA, E., DIMAURO, S. & POWERS, J. M. (1993) Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects. Journal of Neuropathology and Experimental Neurology 52, 1-10
24. STEFFEN, D. J., VESTWEBER, J. G., CASH, W., EL-HAMIDI, M. & LEIPOLD, H. W. (1994) Multifocal subacute necrotizing encephalomyelopathy in Simmental calves. Journal of Veterinary Diagnostic Investigations 6, 466-471
25. SUMMERS, B. A., CUMMINGS, J. F. & DELAHUNTA, A. (1995) Degenerative diseases of the central nervous system. In: Veterinary Neuropathology. L. Duncan. Mosby, St Louis. pp 211-214
26. VALANNE, L., KETONEN, L., MAJANDER, A., SUOMALAINEN, A. & PIHKO, H. (1998) Neuroradiologic findings in children with mitochondrial disorders. American Journal of Neuroradiology 19, 369-377
27. VAN COSTER, R., LOMBES, A., DE VIVO, D. C., CHI, T. L., DODSON, W. E., ROTHMAN, S., ORRECHIO, E. J., GROVER, W., BERRY, G., SCHWARTZ, J. F., HABIB, A. & DIMAURO, S. (1991) Cytochrome c oxidase-associated Leigh syndrome: phenotypic features and pathogenic speculations. Journal of the Neurological Sciences 104, 97-111
28. VAN DER KNAPP, M. S., JAKOBS, C. & VALK, J. (1996) Magnetic resonance imaging in lactic acidosis. Journal of Inherited Metabolic Diseases 19, 535-547
29. VAN ERVEN, P. M. M., CILLESSEN, J. P. M., EEKHOFF, E. M. W., GABREELS, F. J. M., DOESBURG, W. H., LEMMENS, W. A. J. G., SLOOFF, J. L., RENIER, W. O. & RUITENBEEK, W. (1987) Leigh Syndrome, a mitochondrial encephalo(myo)pathy. Clinical Neurology and Neurosurgery 89, 217-230
30. ZEVIANI, M., BERTAGNOLIO, B. & UZIEL, G. (1996) Neurological presentations of mitochondrial diseases. Journal of Inherited Metabolic Diseases 19, 504-520
31. ZEVIANI, M., TIRANTI, V. & PIANTADOSI, C. (1998) Mitochondrial disorders. Medicine 77, 59-72