Adult-onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): a diagnostic challenge.

Neuroimaging Neurology Stroke

Journal

BMJ case reports
ISSN: 1757-790X
Titre abrégé: BMJ Case Rep
Pays: England
ID NLM: 101526291

Informations de publication

Date de publication:
26 Feb 2024
Historique:
medline: 28 2 2024
pubmed: 28 2 2024
entrez: 27 2 2024
Statut: epublish

Résumé

Rare causes of stroke-like presentations can be difficult to diagnose. We report a case of a man in his 40s who first presented with stroke symptoms, but whose clinical course was not typical for a stroke. A detailed investigation of the patient's medical history revealed bilateral sensorineural hearing loss which prompted a wider diagnostic assessment.Furthermore, lack of vascular risk factors and a normal angiogram strengthened our suspicion of an unusual underlying condition. Raised lactic acid levels and genetic analysis confirmed a diagnosis of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.

Identifiants

pubmed: 38413140
pii: 17/2/e256306
doi: 10.1136/bcr-2023-256306
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Jason Acquaah (J)

Neurosciences, University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, UK jason.acquaah@yahoo.co.uk.

Phillip Ferdinand (P)

Neurosciences, University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, UK.

Christine Roffe (C)

Neurosciences, University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, UK.
Stroke Research, Keele University School of Medicine, Keele, UK.

Classifications MeSH