MTHFR gene mutation is the abbreviation of a genetic mutation that affects 30-50 %of society.
Most of us are unaware of whether we carry this mutation.
What is Mthfr? MTHFR specifically, it is a gender that holds a methylengrophidrofolate reduction of our body, an enzyme that helps to convert vitamin B9 to a usable form called -folate -methylpholate.
This process is named after the methylation.
When this gene works properly, it helps our body to convert vitamin B9 into a methylpholate form.
However, when the gene is mutated, the capacity to convert vitamin B9 to methylpholate loses 40 – 70 %.
This gene mutation is important because it is important to convert the folate into a usable form;
DNA synthesis and repair,
Production of neurotransmitter,
And it is vital for immune function.
Researchers have recently discovered various connections between MTHFR mutations and various health problems. Some of these complaints can be listed as follows:
Recurrent abortions during pregnancy
MTHFR mutation varieties have discovered more than 50 MTHFR gene mutation types. Probably there is so much that has not yet been discovered.
However, the most widely examined, encountered and tested types are coded as C677T and A1298C.
MTHFR folic acid relationship is considered harmful to people with MTHFR mutation, a synthetic vitamin found in almost all vitamin supplements.
Folic acid, which is easily absorbed by the body under normal circumstances, cannot be converted into a available form by people with low MTHFR enzyme levels.
What are the symptoms of MTHFR gene mutation? Cardiovascular (blood clots, paralysis, embolism and heart attacks)
Chronic pain and fatigue
Migraine is widely associated with MTHFR.
MTHFR Gene Mutation Test Thanks to its highly consistent special tests, this mutation test can be performed in our country by the health institutions of Kısıklı.
MTHFR gene mutation and pregnancy recurrent miscarriages and neural tube defects are complaints that are thought to be associated with MTHFR.
There is evidence that women with C677T variant have a high risk of having a child with a neural tube defect.
The studies on this subject are still ongoing the research process.
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