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Enevia Health, LLC
30 N Gould Ste N, Sheridan, WY 82801, USA
Genetic expression test.
As a specialist and pioneer in essential and toxic elemental tests, as well as other innovative specialty tests, Doctor's Data offers a wide range of functional tests to aid decision-making and improve patient outcomes.
DNA methylation pathway profiling allows clinicians to screen their patients for a variety of genetic changes (single nucleotide polymorphisms or SNPs) that can affect the function of important biochemical processes such as methionine metabolism, detoxification, hormonal balance, and vitamin D function.
The presence or absence of SNPs can modify the risk of disease. Risks can be reduced by lifestyle changes, and inefficient biochemical processes can be supported by diet and nutritional supplementation to maximize metabolic pathway functions.
IMPORTANT!!! Samples are sent to the US once a month from the Fundación Bioabordajes del Autismo. Check with them the departure dates.
The Doctor's Data DNA methylation pathway profile includes a variety of SNPs that influence many aspects of health, including:
SNPs are DNA sequence variations that occur relatively frequently in the general population. They are different from disease mutations, which are very rare. Huntington's disease is an example of a disease mutation: if you inherit the altered gene, the disease will develop.
Certain SNPs may be associated with particular health conditions, but are not known to directly cause disease. Most SNPs affect the structure and function of cellular proteins, enzymes, or receptors.
The identification of SNPs and their impact on health and physiology is an area of ongoing research; the hope is that finding and studying these small variations in DNA will lead to better and more individualized medical interventions. In many cases, the environment (diet, nutrition, exposure to toxic substances, stress) can further modify gene and SNP expression.
SNPs Affecting Detoxification and Methylation they become even more important if a patient has been exposed to toxic substances such as mercury, lead, or bisphenol A (BPA). Lead and BPA inhibit the function of methyltransferases, and mercury inhibits methionine synthase, an enzyme important in homocysteine remethylation. Methylation is an essential step in the detoxification and elimination of arsenic and other xenobiotics. Normal methionine metabolism is a critical component of Phase II detoxification processes; B-12- and folate-dependent transmethylation and B-6-dependent transsulfuration pathways convert homocysteine to cysteine. Cysteine is an important precursor in the biosynthesis of glutathione.
The greatest difficulty in interpreting SNP results is determining the extent to which a DNA genotype is phenotypically expressed. Functional tests, combined with assessment of patient symptoms and responses to intervention, are necessary to assess the influence of known SNPs on the phenotype.
The plasma methylation profile of DDI is one such test; provides a direct assessment of several major metabolites indicating genetic and epigenetic effects. Plasma methylation profiling is a functional follow-up test when identifying SNPs that affect methionine metabolism.
DDI's DNA methylation pathway profiling allows clinicians to screen their patients for a variety of SNPs that can affect the function of important biochemical processes. Identifying SNPs that influence health and disease risk allows clinicians to support their patients with appropriate lifestyle and nutrition changes to maximize health and wellness.
The studied genes in this test are:
ACAT – 1-02
AHCY-19
AHCY-1
AHCY-2
BHMT-1
BHMT-2
BHMT-4
BHMT-8
CBS–A360A
CBS–C699T
CBS–N212N
COMT-61
COMT-H62H
COMT-V158M
MAO A – R297R
MTHFR–3
MTHFR–A1298C
MTHFR–C677T
MTR-A2756G
MTRR-11
MTRR–A66G
MTRR-H595Y
MTRR-K350A
MTRR-R415T
MTRR-S257T
US – D298E
SHMT–C1420T
SUOX-S370S
VDR–Fok1
VDR–Taq1
The results of each gene will be classified as follows:
Minus "-" does not represent any mutation
Plus "+" represents a mutation
"- / -" indicates no mutation
“+/-” indicates that there is a mutation (it is heterozygous)
«+ / +» Indicates that there is a double mutation (it is homozygous)
You have to contact the collaborating entity you want from your country:
Argentina:
Laboratory IICT LABS
Autism Bioapproach Foundation
Ecuador:
Doctor Oscar Castro
Peru:
GFG Laboratory
Uruguay:
Doctor Antonella Fanetti
Purchase process: contact the collaborating laboratory to manage the test.
ARGENTINA
Laboratory IICT LABS
1220 Miter Street
S2000BHX
ROSARY BEADS
SANTA FE, ARGENTINA.
+543414484517
www.iictlabs.com
iict@iictlabs.com
CUIT: 33-70874216-9
Contact person:
Coordinator Franco Pongelli
+543413201729
fpongelli@iictlabs.com
PERU
GFG Laboratory
El Sauzal Passage. 105 Urb. Los Sauces
(Alt. block 8 av. 8 av. Villarán)
Surquillo, Lime
Peru
+51 989 692 828
Contact person:
Coordinator of Enevia Health in Peru Giovanna Bejerano
+51 983 514 369
Address of attention: Av. Benavides 2426 office 202 Miraflores. Lima 15048
Opening hours: Wednesdays 10:30 am to 12:30 pm.
URUGUAY
Doctor Antonella Fanetti De La Hoz
Office address:
Contact person:
Doctor Antonella Fanetti De La Hoz
Contact number: +598 99 728 557
Mail: antonellafanetti@gmail.com
Hours: 9:00 AM to 3:00 PM
ECUADOR
Doctor Oscar Castro
Contact person:
Enevia Health Coordinator in Ecuador: Doctor Oscar Castro
Mail: nutraautism@gmail.com
Schedule: 09:00 to 20:00
ARGENTINA
Autism Bioapproach Foundation:
Department 1ºC
Juan Agustin Garcia 2780
(1419) Villa, Santa Rita.
CABA, Argentina
Reports: autismobio@gmail.com
+54 11 6825-8726
Studies: bioabordajesdelautismo@hotmail.com
+54 11 5062-0709
Contact person:
adriana peralta
Biomedical nutritional advice
Master of Disability
President of the Autism Bioapproach Foundation.
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30 N Gould Ste N, Sheridan, WY 82801, USA
Our groups are the ideal platform to learn and share your scientific concerns about neurodevelopment issues
*Our purpose is informational only, it is not intended to be a substitute for medical advice, diagnosis or treatment.
This plan is exclusive for people who are responsible for or suffer from some neurodevelopmental pathology such as (TEA, ADD, ADHD, OCD, SLI and other learning disorders, as well as Rett syndrome, Tourette syndrome, PANS, PANDAS , LYME…
With this plan you can benefit from discounts on more than 100 laboratory tests, medical visits, supermarkets and therapies and you will have access to all the tests with the BIGGEST possible discount.
Enevia Health, following its commitment to health and well-being, has created another membership designed for all those people who need these tests and want to benefit from the facilities offered by Enevia.
Subscribe to our HEALTH PLAN and start enjoying the advantages we offer you.
In this modality you will NOT pay annual membership, you will be able to buy on our website but you will not be able to benefit from the discounts that those people subscribed to one of our plans have.
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