Download PDF
Rofo 2024; 196(08): 769-772
DOI: 10.1055/a-2102-0493
Bildessay

Mitochondriale Enzephalomyopathie mit Laktatazidose und Schlaganfall-ähnlichen Episoden (MELAS): Besondere Merkmale in der MRT

Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): Special MRI features
Stefan Heckl
1   Department of Diagnostic and Interventional Neuroradiology, Eberhard Karls University Tübingen, Tübingen, Germany (Ringgold ID: RIN9188)
2   Neuroradiology, Hirslanden Klinik Hirslanden, Zurich, Switzerland (Ringgold ID: RIN30364)
,
Georg Gohla 
1   Department of Diagnostic and Interventional Neuroradiology, Eberhard Karls University Tübingen, Tübingen, Germany (Ringgold ID: RIN9188)
,
Katharina Kneer
3   Department of Neurology, Eberhard Karls University Tübingen, Tübingen, Germany (Ringgold ID: RIN9188)
,
Marius Horger
4   Department of Diagnostic and Interventional Radiology, Eberhard Karls University Tübingen, Tübingen, Germany
› Author Affiliations
› Further Information
Also available at
    Permissions and Reprints

Das Syndrom der Mitochondrialen Enzephalomyopathie mit Laktatazidose und Schlaganfall-ähnlichen Episoden (MELAS) erfasst viele Organe und beruht auf speziellen Mutationen in der mitochondrialen DNA (mtDNA), welche nur durch die Mutter vererbt werden können.



Publication History

Received: 20 May 2023

Accepted: 26 May 2023

Article published online:
19 July 2023

© 2023. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany