Article Text
A difficult case
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) in the older adult
Statistics from Altmetric.com
Footnotes
-
Contributors SA drafted the manuscript. TV, GT, JP and MRT edited the manuscript.
-
Competing interests None.
-
Patient consent Obtained.
-
Provenance and peer review Not commissioned; externally peer reviewed. This paper was reviewed by Patrick Chinnery, Newcastle-upon-Tyne, UK.
Linked Articles
- Editors' choice
Read the full text or download the PDF:
Other content recommended for you
- Clinical mitochondrial genetics
- Mitochondrial disease: mimics and chameleons
- MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity
- Clinical features, investigation, and management of patients with defects of mitochondrial DNA
- Could it be mitochondrial? When and how to investigate
- Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variant
- The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation—implications for diagnosis and management
- Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases
- Mitochondria
- Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies