Well, there is truth to that! There are good genetics and bad genetics. The human genome map identifies the genetic make up of the entire human body. Genome is a fancy word for all your DNA and each genome contains the information needed to build and maintain the human body throughout life! They affect the color of eyes, hair, and skin. More importantly, variations in genome also influence the risk of developing diseases and responses to medications.
The Human Genome Project (HGP) was one of the great feats of exploration in history. Rather than an outward exploration of the planet or the cosmos, the HGP was an inward voyage of discovery led by an international team of researchers looking to sequence and map all of the genes -- together known as the genome -- of members of our species, Homo sapiens. Beginning on October 1, 1990 and completed in April 2003, the HGP gave us the ability, for the first time, to read nature's complete genetic blueprint for building a human being.
Your genome is the operating manual containing all the instructions that helped you develop from a single cell into the person you are today. It guides your growth, helps your organs to do their jobs, and repairs itself when it becomes damaged. And it’s unique to you. The more you know about your genome and how it works, the more you'll understand your own health and make informed health decisions.
A (CGx) carcinogenetic test identifies specific, inheritable gene mutations that may increase a person’s risk of developing or redeveloping cancer. Gain insight as this test will analyzes genes and tumor markers, including BRCA1, BRCA2, ATM, COH1, MLH1, HSH2, MSH6 and PTEN. This website will help you understand how genetics play a role in hereditary cancer and how you can protect you and your family's health with this important information.
Pharmacogenetics test (PGX) focuses on how your body’s drug metabolizing enzymes and provides you with useful insight as to which medications are more useful, less useful and those that are potentially harmful. Pharmacogenetics is the study of how people respond differently to drug therapy based upon their genetic makeup or genes.
Primary immunodeficiencies are a large group of hereditary or genetic disorders that impair the normal functioning of the cells of the immune system, rendering the patient unable to fight infection.
Inherited heart conditions are passed on through families and are caused by a change (or mutation) in one or more of our genes. There are many types of inherited heart conditions, including:
An abnormality of the heart muscle making it harder for the heart to pump blood to the body
An abnormality of the heart rhythm causing the heart to beat too fast, too slow or irregularly
Problems with the structure of the arteries in many parts of the body, including the heart
Familial Hypercholesterolemia (FH)
Causes very high cholesterol from a young age and makes you more likely to get coronary heart disease.
Parkinson's, Alzheimer's and Dementia
Parkinson’s disease, Alzheimer’s disease, and genetic disorders that cause dementia. Genes play a role in the development of many types of dementia. A person with parent or sibling with dementia such as Alzheimer’s disease has on average a higher risk of developing the same condition themselves. Genetic testing can show if you have a specific gene that puts you at risk for developing Alzheimer’s.
The bloom hereditary genetic tests consist of a simple at home cheek swab. Speak with one of our lab representatives for a $0 cost hereditary medical assessment and our medical director will produce a report and recommendation your primary care physician to determine whether a genetic test is medically necessary.
If you are diagnosed with a disease, or if a family history of a disease is revealed through testing, understanding your genetics can help you make more informed treatment decisions. It can also provide insight into how particular predispositions may play a role within your family. That not only includes your children but siblings, aunts, and uncles, nieces and cousins.
Results let you work with your healthcare provider to explore lifestyle changes and medically informed decisions to reduce your health risks. A bloom genetic test increases the probability of early detection, which dramatically increases the rate of survival. There are hundreds of unique genes that can be tested within any one of the bloom genetic tests. A mutation in one or more of these genes can indicate an increased risk of cancer, including breast, ovarian, colorectal or prostate. It could also determine a predisposition towards cardiovascular disease, alzheimers, dementia or parkinson's disease. Pharmacogenetics test can determine how you respond to drug therapy based upon your genetic makeup or genes.
There's much to see here. So, take your time, look around, and learn all there is to know about the bloom hereditary genetic testing. You can also call our customer service hotline if you have any further questions at 877-706-GENE (4363).
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