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POLG1manifestations in childhood

Authors :
Isohanni, P.
Hakonen, A.H.
Euro, L.
Paetau, I.
Linnankivi, T.
Liukkonen, E.
Wallden, T.
Luostarinen, L.
Valanne, L.
Paetau, A.
Uusimaa, J.
Lönnqvist, T.
Suomalainen, A.
Pihko, H.
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