By Philip M. Parker
In March 2001, the nationwide Institutes of overall healthiness issued the next caution: "The variety of websites providing health-related assets grows each day. Many websites supply priceless details, whereas others could have info that's unreliable or misleading." additionally, due to the speedy bring up in Internet-based details, many hours may be wasted looking out, deciding on, and printing. for the reason that in simple terms the smallest fraction of knowledge facing Alexander disorder is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web examine may be not just time eating, but additionally incomplete. This publication was once created for doctors, scholars, and participants of most people who are looking to behavior clinical examine utilizing the main complex instruments to be had and spending the smallest amount of time doing so.
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Extra info for Alexander Disease - 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.
Are Chromosomal Disorders Inherited? Although it is possible to inherit some types of chromosomal abnormalities, most chromosomal disorders (such as Down syndrome and Turner syndrome) are not passed from one generation to the next. Some chromosomal conditions are caused by changes in the number of chromosomes. These changes are not inherited, but occur as random events during the formation of reproductive cells (eggs and sperm). An error in cell division called nondisjunction results in reproductive cells with an abnormal number of chromosomes.
These molecules identify which copy of a gene was inherited Help Me Understand Genetics 45 from the mother and which was inherited from the father. The addition and removal of methyl groups can be used to control the activity of genes. Only a small percentage of all human genes undergo genomic imprinting. Researchers are not yet certain why some genes are imprinted and others are not. They do know that imprinted genes tend to cluster together in the same regions of chromosomes. Two major clusters of imprinted genes have been identified in humans, one on the short (p) arm of chromosome 11 (at position 11p15) and another on the long (q) arm of chromosome 15 (in the region 15q11 to 15q13).
Alexander Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker