NX GEN SEQ, FAMILIAL HEMIPLEGIC MIGRAINE
Familial hemiplegic migraine (FHM) is a common cause of headache that runs in families. Migraines usually cause episodic headache associated with nausea, vomiting, sensitivity to light and sound. Migraine attack has 3 phases namely- prodrome phase, headache phase & postdrome phase. About 20-25% patients have 4th phase called aura phase. Mutations in the CACNA1A, ATP1A2, SCN1A & PRRT2 genes have been found to cause FHM. The first three genes provide instructions for making proteins involved in the transport of charged ions across cell membranes. Function of the protein produced from the PRRT2 gene is unknown, although studies suggest it interacts with a protein that helps control signaling between neurons.
Parameter(s) covered : 1
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Parameters
- Nx GEN SEQ FAMILIAL HEMIPLEGIC MIGRAINE