Neuropathology in Kearns-Sayre syndrome

Acta Neuropathologica

Volumn 80, Issue 5, 1990, Pages 541-546

  Oldfors, A ^a   Fyhr, I M ^a   Holme, E ^a   Larsson, N G ^a   Tulinius, M ^a  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

Author keywords

Central nervous system; Mitochondria; Pathology; Skeletal muscle

Indexed keywords

ADULT; ARTICLE; AUTOPSY; BASAL GANGLION; CASE REPORT; CAUDATE NUCLEUS; GLIOSIS; GLOBUS PALLIDUS; HISTOLOGY; HUMAN; KEARNS SAYRE SYNDROME; MALE; MITOCHONDRIAL MYOPATHY; NERVE CELL DEGENERATION; PRIORITY JOURNAL; ULTRASTRUCTURE;

ADULT; BASAL GANGLIA; BRAIN STEM; CASE REPORT; CENTRAL NERVOUS SYSTEM; CEREBELLUM; CEREBRAL CORTEX; CHROMOSOME DELETION; DNA, MITOCHONDRIAL; HUMAN; KEARNS SYNDROME; MALE; MESENCEPHALON; MITOCHONDRIA, MUSCLE; SPINAL CORD; SUPPORT, NON-U.S. GOV'T; THALAMUS;

EID: 0024987489     PISSN: 00016322     EISSN: 14320533     Source Type: Journal    
DOI: 10.1007/BF00294616     Document Type: Article

References (27)

1. Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia
2. Lumping or splitting? “Ophthalmoplegia plus” or Kearns-Sayre syndrome?
3. Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological and biochemical studies in muscle biopsies and autopsy tissue
4. Hypoxia and vascular disorders of the central nervous system
5. Ophtalmoplégie externe progressive avec spongiose des noyaux du tronc cérébral
6. Etude anatomo-clinique d'une observation d'“Ophtalmoplegia plus” avec analyse des lésions musculaires, nerveuses centrales, oculaires, myocardiques et thyroidiennes
7. Heart block in Kearns-Sayre syndrome. Electrophysiologic-pathologic correlation
8. Spongiform encephalopathy with chronic progressive external ophthalmoplegia. Central ophthalmoplegia mimicking ocular myopathy
9. Mitochondrial myopathies
10. Carbon monoxide
11. Demyelinating radiculopathy in the Kearns-Sayre syndrome: a clinicopathological study
12. Eigenartige Erkrankung im extrapyramidalen System mit besonderer Beteiligung des Globus pallidus und der Substantia nigra
13. Kearns-Sayre syndrome with hypoparathyroidism
14. Occurrence of retinal pigmentation, ophthalmoplegia, ataxia, deafness, and heart block
15. The spread of brain oedema in hypertensive brain injury
16. Retinitis pigmentosa, external ophthalmoplegia, and complete heart block
17. Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome
18. Kearns-Sayre syndrome with muscle DNA deletion
19. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
20. Cytochrome c oxidase deficiency in infancy
21. Intracerebral distribution of mitochondrial abnormalities in 21 cases of infantile spongy dystrophy
22. Edema in neurotoxic injury
23. Diverse clinical disorders associated with morphological abnormalities of mitochondria
24. Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue
25. Deletions of mitochondrial DNA in Kearns-Sayre syndrome