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- ... GRACILE syndrome Gaucher disease Glycogen storage disease type I Hereditary fructose intolerance Junctional epidermolysis bullosa Leigh syndrome ...
- Before undergoing genetic testing, it is important to be sure that the test is valid and useful. A genetic test is valid if it provides an accurate result. ...
- If you are interested in direct-to-consumer genetic testing, do some research into the companies that offer these services. Questions that can help you ...
- While a direct-to-consumer genetic test can estimate your risk, it cannot tell you for certain whether you will or will not develop certain forms of cancer. ...
- While a direct-to-consumer genetic test can estimate your risk, it cannot tell you for certain whether you will or will not develop Alzheimer's disease . Variations ...
- To find a genetics professional in your community, you may wish to ask your doctor for a referral. If you have health insurance, you can also contact your ...
- Mucopolysaccharidosis type I (MPS I) is a condition that affects many parts of the body. This disorder was once divided into three separate syndromes: Hurler syndrome (MPS I- ...
- Glutaric acidemia type I (also called glutaric aciduria type I) is an inherited disorder in which the body is unable to process certain proteins properly. It is ...
- Carnitine palmitoyltransferase I (CPT I) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without ...
- Carbamoyl phosphate synthetase I deficiency is an inherited disorder that causes ammonia to accumulate in the blood (hyperammonemia). Ammonia, which is formed when ...