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MELAS, an important consideration in the adult population presenting with unusual and recurrent stroke-like episodes.
Corr, Alison; Gaughan, Maria; Moroney, Joan; Looby, Seamus.
Afiliación
  • Corr A; Department of Radiology, Beaumont Hospital, Dublin, Ireland.
BMJ Case Rep ; 20142014 Jan 28.
Article en En | MEDLINE | ID: mdl-24473421
A 48-year-old man was admitted for workup of stroke-like symptoms and generalised tonic-clonic seizures. History and examination revealed that the patient had background diagnoses of type 2 diabetes mellitus, epilepsy and had suffered a temporal lobe infarct 3 years ago. The unusual presentation and physical findings, along with subsequent MRI findings led to a diagnosis of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). MELAS is a mitochondrial disorder typified by the aforementioned symptoms, and is typically diagnosed in the first two decades of life.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encéfalo / Imagen por Resonancia Magnética / Síndrome MELAS Tipo de estudio: Diagnostic_studies Límite: Humans / Male / Middle aged Idioma: En Revista: BMJ Case Rep Año: 2014 Tipo del documento: Article País de afiliación: Irlanda Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encéfalo / Imagen por Resonancia Magnética / Síndrome MELAS Tipo de estudio: Diagnostic_studies Límite: Humans / Male / Middle aged Idioma: En Revista: BMJ Case Rep Año: 2014 Tipo del documento: Article País de afiliación: Irlanda Pais de publicación: Reino Unido