Newvit

Avoiding Vitiligo ...

The code has been cracked!

Codes are developed not to be cracked.
But scientists are curious to find answers to so many questions that appear.
Reading our DNA, analyzing it and finding the errors that lead to diseases is one of the discoveries of the century.

The change of a single letter or nitrogenous base is responsible for predisposing us to Vitiligo in its generalized form.

Today everyone must analyze their DNA sequencing and detect or rule out variants and their risk genotypes.

As more people take this important study, the more accurate the results will be.
It is very easy to perform this analysis. A sample of saliva is used. You can receive in your country and at home the special plastic tube for that purpose.

. . CGA TAT TCC C*A*T CGA TC. . (L155H A>T 17p13.2) is part of the code!

How does it benefit you?
Knowing if you have that code benefits you in every possible way. A specific example: You already have Vitiligo, so you can tell if it will tend to be generalized and difficult. You don't have Vitiligo yet, but a relative does have it, so it helps you know if you received it in your inheritance and if you can have it at some point in your life. Another concrete example, you do not present Vitiligo nor do you have relatives that you know who have it, so know if you have the code to develop Vitiligo and other diseases at some time in your life. You should know your carrier status and that mean, it without have Vitiligo disease, but you can transmit it to your children. More importantly for all possible scenarios, knowing that you present this risk, it can be modified to keep it methylated so that it is not expressed and Vitiligo or new Vitiligo spots are avoided. In many ways it benefits you to know.