Download Jervell and Lange-Nielsen Syndrome - A Bibliography and by Philip M. Parker PDF

By Philip M. Parker

In March 2001, the nationwide Institutes of health and wellbeing issued the next caution: "The variety of websites supplying health-related assets grows on a daily basis. Many websites offer useful info, whereas others could have details that's unreliable or misleading." in addition, end result of the speedy raise in Internet-based info, many hours will be wasted looking, identifying, and printing. due to the fact in basic terms the smallest fraction of data facing Jervell and Lange-Nielsen syndrome is listed in se's, similar to www.google.com or others, a non-systematic method of net learn will be not just time eating, but additionally incomplete. This e-book was once created for doctors, scholars, and contributors of most people who are looking to behavior scientific study utilizing the main complex instruments on hand and spending the smallest amount of time doing so.

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Extra resources for Jervell and Lange-Nielsen Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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X-linked recessive inheritance: Because of the difference in sex chromosomes, the probability of passing on an X-linked recessive disorder also differs between men and women. The sons of a man with an X-linked recessive disorder will not be affected, and his daughters will carry one copy of the mutated gene. With each pregnancy, a woman who carries an X-linked recessive disorder has a 50 percent chance of having sons who are affected and a 50 percent chance of having daughters who carry one copy of the mutated gene.

Other conditions, such as Beckwith-Wiedemann syndrome (a disorder characterized by accelerated growth and an increased risk of cancerous tumors), are associated with abnormalities of imprinted genes on the short arm of chromosome 11. 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.

Down syndrome is an example of a condition caused by trisomy—people with Down syndrome typically have three copies of chromosome 21 in each cell, for a total of 47 chromosomes per cell. Monosomy, or the loss of one chromosome from each cell, is another kind of aneuploidy. “Mono-” is Greek for “one”; people with monosomy have one copy of a particular chromosome in each cell instead of the normal two copies. Turner syndrome is a condition caused by monosomy. Women with Turner syndrome are often missing one copy of the X chromosome in every cell, for a total of 45 chromosomes per cell.

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