Nutrigenomics: The study of how different foods may interact with specific genes to increase the risk of common chronic diseases such as type 2 diabetes, obesity, heart disease, stroke and certain cancers. Nutrigenomics : A science which studies the interplay of food and DNA, and helps us design right diet and exercise regimens
Evaluate your genes
Improvement of your diet and lifestyle
Secure fut
ure health risk
Buffer (solution in the test tube) used to keep DNA stable, has been developed and patented by us
Analysis takes 18 to 21 days. Counseling covers dietary and fitness regime, individual is informed about his/her own genetic makeup and genes and conditions
Process to give sample
Kit has a bottle with solution in it. about 30 milliliters of saliva is required. Seal up your sample and place it in the conveniently provided preaddressed envelope. Mail it and we will get back to you with your results. Reports
Pre Test Sessions
Post Test Sessions
Diet Counselling Exercise Counselling
Introduction of Nutrigenomics:
Mouthful of spit contains hundreds of complex protein molecules -- what scientists call enzymes (Help in the digestion of food)
Swirling around with those enzymes are cells shed off from the inside of your cheek. Inside each of those cells lies a nucleus, and inside each nucleus, chromosomes
Chromosomes themselves are made up of DNA(deoxyribonucleic acid) the double-stranded molecule that gets much of the credit for what we look like and how we act
How test is done
Using the extensive databases and associated research, testing companies can predict your risk of developing certain diseases based on what gene variants are present in your code. You’ll receive comprehensive reports outlining your risk factors for each disease, along with your carrier status and additional information explaining how to interpret the results. Experts will recommend dietary + exercise do’s and don'ts
Why genetic test:
Carrier screening tells you whether you carry a genetic variant associated with certain genetic disorders. Most of the time, these variants will not affect you directly, but you may pass them on to your children. Examples include Diabetes, Obesity, cystic fibrosis, sickle cell anemia, and hereditary hearing loss. Most commonly, if both parents are carriers for a certain disease-causing variant, there will be a 25% chance that their child will be affected by the disease
