Back to Search
Start Over
Adult onset Leigh syndrome with mitochondrial DNA 8344 A>G mutation.
- Source :
-
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia [J Clin Neurosci] 2014 Nov; Vol. 21 (11), pp. 2009-11. Date of Electronic Publication: 2014 Jun 21. - Publication Year :
- 2014
-
Abstract
- We report a pedigree of adult-onset Leigh syndrome (LS) with mitochondrial mutation 8344 A>G. A 38-year-old woman presented with optic neuropathy, weakness and cognitive impairment. Family history of optic neuropathy and systemic involvement was suggestive of mitochondrial encephalopathy. Genetic and radiologic studies showed m.8344 A>G mutation with characteristics of LS. To our knowledge this is the first case of adult-onset LS demonstrating the m.8344 A>G mutation.<br /> (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Subjects :
- Adenine
Adult
Age of Onset
Cognitive Dysfunction genetics
Diffusion Magnetic Resonance Imaging
Female
Genetic Testing
Guanine
Humans
Leigh Disease pathology
Memory Disorders genetics
Muscle Weakness genetics
Optic Atrophies, Hereditary pathology
Brain pathology
DNA, Mitochondrial genetics
Leigh Disease diagnosis
Leigh Disease genetics
Mutation
Optic Atrophies, Hereditary diagnosis
Optic Atrophies, Hereditary genetics
Pedigree
Subjects
Details
- Language :
- English
- ISSN :
- 1532-2653
- Volume :
- 21
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
- Publication Type :
- Academic Journal
- Accession number :
- 24961732
- Full Text :
- https://doi.org/10.1016/j.jocn.2014.03.020