A thorough understanding of human genetics holds the promise to drastically modify healthcare through personalized preventative treatments and care. In an age where information is instantly available, it comes as no surprise that people wish to know as much as possible about their risk of catching certain diseases. Genetic testing using blood, inside of the cheek or saliva may signal susceptibilities to various health conditions, and help determine the chances of developing a certain illness.

The ratio of our health affected by our heredities and the effect of our environment and behavior depends on specific conditions. While some illnesses are completely genetic (cystic fibrosis, Huntington’s disease, Tay-Sachs, Down syndrome, and sickle cell anemia) and 100% penetrant, others are more complex and have a substantial behavioral element, such as rheumatoid arthritis or Type-2 diabetes. What this means is if an individual has a hereditary predisposition towards a certain disease, there is so much one can do in terms of behavior to prevent it.

DNA testing identifies changes in genes, proteins, or chromosomes. The array of genetic tests has increased over the years. At present, these tests involve assessing several genes to identify the risk of developing certain disorders or diseases, with the more common diseases comprising of cancer and heart disease. The outcome of a DNA test can verify or chart out a potential genetic condition or help determine an individual’s chance of getting or passing on a genetic disease. Hundreds of DNA tests are used currently, and more are being developed with every passing day.

The procedure is also used to analyze hereditary disorders in both newborn babies and parents in hospitals across the world. These maladies include hemophilia, cystic fibrosis, Huntington’s disease, familial Alzheimer’s, thalassemia, and many others.

Early discovery of ailments allows medical experts to help parents prepare for an appropriate treatment plan for the child. In some programs, genetic counselors use DNA testing data to help future parents realize the peril of an affected child. In other programs, future parents use DNA testing information in their decisions regarding affected pregnancies.

Research programs designed to detect inherited illnesses on the chromosomes depends on the information present in DNA fingerprints. Through studying the DNA fingerprints of folks who have a history of some specific disorder, or by linking large groups of people with and without the illness, it is probable to find DNA patterns linked with the disease at hand. This work is an essential first step in crafting an ultimate genomic cure for these diseases.

In short, DNA testing can not only provide you information about potential diseases you may be at risk of but it can also show the carrier status of certain mutations that you may pass on to your children. To find more about your health status, Contact us today and schedule an appointment with the best DNA Testing Center in all of NYC!

please call us at 718-701-0292 to schedule an appointment with the top DNA testing center in NYC.