Abstract | BACKGROUND: METHODS: We evaluated the clinical characteristics in a patient with a neonatal-onset complex episodic neurologic phenotype. We screened SCN2A for mutations and carried out in vitro electrophysiologic analyses to study the consequences of the identified mutation. We studied the developmental expression of Na(V)1.2 in cerebellum by immunohistochemical analysis. RESULTS: The patient presented with neonatal-onset seizures and variable episodes of ataxia, myoclonia, headache, and back pain after 18 months of age. The patient carries a de novo missense mutation (p.Ala263Val) in SCN2A, which leads to a pronounced gain-of-function, in particular an increased persistent Na(+) current. Immunohistochemical studies suggest a developmentally increasing expression of Na(V)1.2 in granule cell axons projecting to Purkinje neurons. CONCLUSIONS: These results can explain a neuronal hyperexcitability resulting in seizures and other episodic symptoms extending the spectrum of SCN2A-associated phenotypes. The developmentally increasing expression of Na(V)1.2 in cerebellum may be responsible for the later onset of episodic ataxia.
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Authors | Y Liao, A-K Anttonen, E Liukkonen, E Gaily, S Maljevic, S Schubert, A Bellan-Koch, S Petrou, V E Ahonen, H Lerche, A-E Lehesjoki |
Journal | Neurology
(Neurology)
Vol. 75
Issue 16
Pg. 1454-8
(Oct 19 2010)
ISSN: 1526-632X [Electronic] United States |
PMID | 20956790
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- NAV1.2 Voltage-Gated Sodium Channel
- Nerve Tissue Proteins
- SCN2A protein, human
- Scn2a protein, mouse
- Sodium Channels
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Topics |
- Age Factors
- Animals
- Animals, Newborn
- Ataxia
(complications, genetics)
- Cell Line, Transformed
- Cerebellum
(growth & development, metabolism, pathology)
- Child
- Disease Progression
- Electroencephalography
(methods)
- Epilepsy
(complications, genetics)
- Gene Expression Regulation, Developmental
- Genome-Wide Association Study
(methods)
- Humans
- Magnetic Resonance Imaging
- Membrane Potentials
(genetics)
- Mice
- Mutation
(genetics)
- Myoclonus
(complications, genetics)
- NAV1.2 Voltage-Gated Sodium Channel
- Nerve Tissue Proteins
(genetics, metabolism)
- Neurons
(metabolism)
- Pain
(complications, genetics)
- Patch-Clamp Techniques
(methods)
- Sodium Channels
(genetics, metabolism)
- Transfection
(methods)
- Video Recording
(methods)
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