Side Effect of Genetic Screening

Genetic screening is the process of analyzing DNA samples to detect the presence of one or more genes associated with hereditary diseases (Genetic Screening 2011). In order to determine the opportunity for a person to develop a genetic disease, the result of a genetic test can exclude a suspected genetic condition (what is a genetic test2011). It will help infertility to have the next generation in the future. In addition, genetic screening is done for several common reasons, including non-genetic screening for disease health and disease prevention.

It is expected that these genetic screenings will become part of the future daily health care and help healthcare providers design effective prevention strategies and treatment options. However, the genetic information must be protected to avoid discrimination against those who may already be vulnerable. In May 2008, a new federal law to protect individuals from individual discrimination by health insurance companies and employers was enacted. It came into force for health insurance companies in May 2009 and came into force for employers in November 2009 (public information discrimination law, public law, 2008). This law, known as Genetic Information Non-Discrimination Act (GINA), allows individuals to perform genetic testing without any discrimination and to be free to participate in research without the need to disclose health insurance or genetic information to health insurance Guaranteed. Employer

Genetic testing and gene screening are two different programs. Genetic testing is a test used to detect the presence of specific gene sequences, chromosomes or gene products related to genetic diseases. Genetic screening of all populations or individuals not necessarily at risk. For example, if you do not have breast cancer in your home and still want to take exams, you will be genetically screened. This is usually done before signs of illness appear. Genetic testing is a program that can be used to judge the identity of diseases such as Crohn's disease and Alzheimer's disease and to judge how high your disease has changed. You can do this to understand or compare partner compatibility. Perform genetic screening to determine if a person can transmit hereditary diseases even if he or she does not have the risk of developing a physical condition

Let's fast forward towards the 2000s when screening newborn babies effectively and obtaining more genetic conditions than PKU. Indeed, we can test dry spots of blood with hundreds of genetic conditions. What is the genetic condition for your baby to be screened as a newborn? Interestingly, that is the date on which your baby was born and on the first day after birth, the baby is officially handed over (if you are in the United States). Due to deciding to add conditions to newborn screening in each state, the number of genetic conditions examined at each newborn's dry blood spot varies from state to state. Currently, the number of diseases in each state ranges from 39 to over 50 genetic conditions. This means that if you have a child in Utah last year, because you live in New York, newborns will be screened under various conditions.