CareLit · DOI-Nachweis · Aktuelle Neurologie
Multiple mtDNA deletions with clinical features resembling MNGIE: a combined MRT/MRS and FDG-PET study
DOI 10.1055/s-2006-953464
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Autor:innenF.G. Lehnhardt, R. Horvath, R. Ullrich, U. Möller-Hartmann, W.F. Haupt
ZeitschriftAktuelle Neurologie
Ausgabe09/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Mitochondrial neurogastrointestinal encephalomyelopathy syndrome (MNGIE) disease is known to present with a homogenous clinical picture. The combination of chronic progressive ophthalmoparesis (CPEO) and gastrointestinal symptoms such as chronic diarrhea, intestinal obstructions and cachexia are considered to be of high diagnostic specificity. Multiple deletions and/or depletion in muscular mitochondrial (mt) DNA we…
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Zitierempfehlung
F.G. Lehnhardt, R. Horvath, R. Ullrich, U. Möller-Hartmann, W.F. Haupt (2006) Multiple mtDNA deletions with clinical features resembling MNGIE: a combined MRT/MRS and FDG-PET study. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2006-953464
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