| Literature DB >> 3727928 |
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.Entities:
Mesh:
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