POLG1 manifestations in childhood
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Abstract
Objective: Mitochondrial DNA polymerase γ (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 POLG1 mutations in neurologic manifestations in childhood.
Methods: We investigated POLG1 in 136 children, all clinically suspected to have mitochondrial disease, with one or more of the following: ataxia, axonal neuropathy, severe epilepsy without known epilepsy syndrome, epileptic encephalopathy, encephalohepatopathy, or neuropathologically verified Alpers syndrome.
Results: Seven patients had POLG1 mutations, and all of them had severe encephalopathy with intractable epilepsy. Four patients had died after exposure to sodium valproate. Brain MRI showed parieto-occipital or thalamic hyperintense lesions, white matter abnormality, and atrophy. Muscle histology and mitochondrial biochemistry results were normal in all.
Conclusions: POLG1 analysis should belong to the first-line DNA diagnostic tests for children with an encephalitis-like presentation evolving into epileptic encephalopathy with liver involvement (Alpers syndrome), even if brain MRI and morphology, respiratory chain activities, and the amount of mitochondrial DNA in the skeletal muscle are normal. POLG1 analysis should precede valproate therapy in pediatric patients with a typical phenotype. However, POLG1 is not a common cause of isolated epilepsy or ataxia in childhood.
Footnotes
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Study funding: Supported by the Jane and Aatos Erkko Foundation, Sigrid Juselius Foundation, Academy of Finland, University of Helsinki (A.S.), Helsinki University Central Hospital EVO grants (A.S. and H.P.), and Biomedicum Helsinki Foundation (A.H.H.).
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- MIRAS
- mitochondrial recessive ataxia syndrome
- mtDNA
- mitochondrial DNA
- POLG
- polymerase gamma
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Supplemental data at www.neurology.org
- Received May 17, 2010.
- Accepted November 15, 2010.
- Copyright © 2011 by AAN Enterprises, Inc.
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