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Noctunal Epilepsy

Noctunal Epilepsy
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Nocturnal epilepsy is inherited in autosomal dominant pattern and is genetically heterogenous. This test reports pathogenic variants in clinically important loci such as calcium channel (CACN), sodium channel (SCN) and acetylcholine receptor (CHRN) family of genes among others. Molecular analysis is done by screening for these mutations, which is required for diagnosis.

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This test is based on Next Generation Sequencing (NGS) and sequences the an entire panel of genes that are linked with the disease.

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