By Philip M. Parker
In March 2001, the nationwide Institutes of wellbeing and fitness issued the next caution: "The variety of websites supplying health-related assets grows each day. Many websites offer invaluable info, whereas others could have details that's unreliable or misleading." moreover, a result of quick elevate in Internet-based details, many hours could be wasted looking, opting for, and printing. considering in basic terms the smallest fraction of data facing Biotinidase deficiency is listed in se's, comparable to www.google.com or others, a non-systematic method of net examine will be not just time eating, but in addition incomplete. This e-book was once created for doctors, scholars, and contributors of most of the people who are looking to behavior clinical learn utilizing the main complex instruments to be had and spending the smallest amount of time doing so.
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Additional resources for Biotinidase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
In addition, some people with a disease-causing mutation never develop any health problems or may experience only mild symptoms of the disorder. If a disease that runs in a family does not have a clear-cut inheritance pattern, predicting the likelihood that a person will develop the condition can be particularly difficult. Estimating the chance of developing or passing on a genetic disorder can be complex. Genetics professionals can help people understand these chances and help them make informed decisions about their health.
Cystic fibrosis, sickle cell anemia X-linked dominant X-linked dominant disorders are caused by mutations in genes on the X chromosome. Females are more frequently affected than males, and the chance of passing on an X-linked dominant disorder differs between men and women. Families with an X-linked dominant disorder often have both affected males and affected females in each generation. A striking characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons (no male-to-male transmission).
A family history also can provide information about the risk of rarer conditions caused by mutations in a single gene, such as cystic fibrosis and sickle cell anemia. While a family medical history provides information about the risk of specific health concerns, having relatives with a medical condition does not mean that an individual will definitely develop that condition. On the other hand, a person with no family history of a disorder may still be at risk of developing that disorder. Knowing one’s family medical history allows a person to take steps to reduce his or her risk.