Types Of Familial Hemiplegic Migraine ?
If a person suffers from temporary paralysis of one part of the body due to genetic mutations, such migraine is called familial hemiplegic migraine. Only born children can be affected by genes For this reason, “familial” addition has been made with the name of such migraine. Familial hemiplegic migraine there are four types which are as follows.
FHM1 Familial hemiplegic is the first and most important type of migraine. There is a gene in our body called CANA1A , CANA1A provides the brain with instructions to make a specific protein. This particular protein is called the alpha-1A subunit of a calcium channel. This calcium channel is important for regulating the flow of calcium ions into nerve cells. Mutations in this gene disrupt normal calcium signaling, This results in nerve cells acting abnormally and triggering migraines. So we call such a migraine FHM1 . In short, if a person starts experiencing severe pain in one part of the head due to a change in CANA1A then it is FHM1 .
FHM 2 Familial hemiplegic is the other main type of migraine due to which the patient feels weakness and numbness on the right or left side of his body.There is a special gene in our body called ATP1A2 . A mutation in ATP1A2 may predispose an individual to familial hemiplegic migraine. And such a migraine is called FHM 2 .
In simple words, it can be said that due to changes in ATP1A2 , a severe throbbing headache starts in one part of a person’s head. Hence such headache is called FHM 2 and is a sub-branch of Familial hemiplegic migraine .
FHM 2 Familial hemiplegic is a subtype of migraine that has a genetic cause and causes temporary paralysis. There is a special gene in our body called SCN1A .
This gene gives instructions for a specific protein.
This protein plays an important role in the functioning of nerve cells, especially in the brain Due to mutations in SCN1A , the individual becomes susceptible to a subtype of Familial hemiplegic Calles FHM 3 .
FHM 4 Familial hemiplegic is the fourth subtype of migraine in which the patient feels that half of his body is paralyzed. Its cause is genetic due to which the patient experiences severe headache.
There is a gene called PRRT2 in our body , this gene releases instructions to make a specific protein. Which works to maintain communication between the nerve cells of the brain.
A subtype of familial hemiplegic migraine may be triggered in an individual by mutations in the PRRT2 gene.
In simple words, we can say that due to changes in PRRT2, severe pain starts in one part of a person’s head, so such a headache is called FHM 4 .
Miracle Tips for Migraines
Remember that there are many types of migraine, all of which are incurable. But by adopting a better diet, better lifestyle, contact with a doctor, and ancient remedies to boost immunity, you can greatly reduce future damage. So if you want to bring peace and happiness in your life visit the below links.
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