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POLG1manifestations in childhood
- Source :
- Neurology (Ovid); March 2011, Vol. 76 Issue: 9 p811-815, 5p
- Publication Year :
- 2011
-
Abstract
- Mitochondrial DNA polymerase (POLG1) mutations in children often manifest as Alpers syndrome, whereas in adults, a common manifestation is mitochondrial recessive ataxia syndrome (MIRAS) with severe epilepsy. Because some patients with MIRAS have presented with ataxia or epilepsy already in childhood, we searched for POLG1mutations in neurologic manifestations in childhood.
Details
- Language :
- English
- ISSN :
- 00283878 and 1526632X
- Volume :
- 76
- Issue :
- 9
- Database :
- Supplemental Index
- Journal :
- Neurology (Ovid)
- Publication Type :
- Periodical
- Accession number :
- ejs49021754
- Full Text :
- https://doi.org/10.1212/WNL.0b013e31820e7b25