Literature DB >> 3727928

Late-onset hereditary myopathy with abnormal mitochondria and progressive dementia.

S T Vilming, P Dietrichson, M M Isachsen, L Løvvik, A Heiberg.   

Abstract

A family with autosomal dominant late-onset progressive dementia and myopathy is described. Electron microscopy of muscle revealed abnormal mitochondria in the proband. Thus, the disease may be classified as a "mitochondrial encephalomyopathy". The cases are unique because dementia was a dominating feature and because the symptoms developed late in life. These cases may represent a new subgroup of the mitochondrial encephalomyopathies.

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Year:  1986        PMID: 3727928     DOI: 10.1111/j.1600-0404.1986.tb04594.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  2 in total

Review 1.  Mitochondrial myopathy: a genetic study of 71 cases.

Authors:  A E Harding; R K Petty; J A Morgan-Hughes
Journal:  J Med Genet       Date:  1988-08       Impact factor: 6.318

2.  Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging.

Authors:  Perry G Ridge; Taylor J Maxwell; Spencer J Foutz; Matthew H Bailey; Christopher D Corcoran; JoAnn T Tschanz; Maria C Norton; Ronald G Munger; Elizabeth O'Brien; Richard A Kerber; Richard M Cawthon; John S K Kauwe
Journal:  BMC Bioinformatics       Date:  2014-05-28       Impact factor: 3.169

  2 in total

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