Literature DB >> 1906933

Stroke-like episodes in familial mitochondrial encephalomyopathy: clinical and biochemical aspects.

M S Damian1, H Reichmann, H J Schütz, W Dorndorf, W Schachenmayr.   

Abstract

Acute episodes of focal neurological dysfunction are a well-recognized complication of the mitochondrial encephalomyopathies. Because of rapid remission, biochemical tests and other diagnostic procedures are mostly performed after the acute phase. We report the case of a patient suffering from mitochondrial disease manifesting primarily with seizures, progressive deafness and dementia, who experienced multiple stroke-like episodes. Other members of the family with evidence of mitochondrial dysfunction are presented briefly. EEG and biochemical findings in the acute stage are correlated with clinical symptoms, showing characteristics distinct from the chronic illness. The possible involvement of dietary factors in the provocation of stroke-like episodes is discussed and regulation of glucose intake suggested as a strategy in the prevention of stroke-like episodes.

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Mesh:

Year:  1991        PMID: 1906933     DOI: 10.1007/bf00315686

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  16 in total

1.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.

Authors:  M Yamamoto; T Sato; M Anno; H Ujike; M Takemoto
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-11       Impact factor: 10.154

2.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Authors:  S G Pavlakis; P C Phillips; S DiMauro; D C De Vivo; L P Rowland
Journal:  Ann Neurol       Date:  1984-10       Impact factor: 10.422

3.  Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions.

Authors:  M Kuriyama; H Umezaki; Y Fukuda; M Osame; K Koike; J Tateishi; A Igata
Journal:  Neurology       Date:  1984-01       Impact factor: 9.910

4.  Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis.

Authors:  Y Kobayashi; S Miyabayashi; G Takada; K Narisawa; K Tada; T Y Yamamoto
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

5.  Independence of blood and cerebrospinal fluid lactate.

Authors:  J B Posner; F Plum
Journal:  Arch Neurol       Date:  1967-05

6.  The cerebral metabolism of glucose and oxygen measured with positron tomography in patients with mitochondrial diseases.

Authors:  R S Frackowiak; S Herold; R K Petty; J A Morgan-Hughes
Journal:  Brain       Date:  1988-10       Impact factor: 13.501

7.  Sensitivity to carbohydrate in a patient with familial intermittent lactic acidosis and pyruvate dehydrogenase deficiency.

Authors:  S D Cederbaum; J P Blass; N Minkoff; W J Brown; M E Cotton; S H Harris
Journal:  Pediatr Res       Date:  1976-08       Impact factor: 3.756

8.  Ketonic diet in the management of pyruvate dehydrogenase deficiency.

Authors:  R E Falk; S D Cederbaum; J P Blass; G E Gibson; R A Kark; R E Carrel
Journal:  Pediatrics       Date:  1976-11       Impact factor: 7.124

Review 9.  Diabetes mellitus in Kearns-Sayre syndrome.

Authors:  Y Tanabe; S Miyamoto; Y Kinoshita; K Yamada; N Sasaki; E Makino; H Nakajima
Journal:  Eur Neurol       Date:  1988       Impact factor: 1.710

10.  Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.

Authors:  N Fukuhara; S Tokiguchi; K Shirakawa; T Tsubaki
Journal:  J Neurol Sci       Date:  1980-07       Impact factor: 3.181

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