Download Carnitine Palmitoyltransferase II Deficiency - A by Philip M. Parker PDF

By Philip M. Parker

In March 2001, the nationwide Institutes of wellbeing and fitness issued the subsequent caution: "The variety of websites supplying health-related assets grows each day. Many websites supply useful info, whereas others can have info that's unreliable or misleading." additionally, as a result of the quick raise in Internet-based details, many hours may be wasted looking, identifying, and printing. when you consider that in basic terms the smallest fraction of data facing Carnitine palmitoyltransferase II deficiency is listed in se's, similar to www.google.com or others, a non-systematic method of web study should be not just time eating, but additionally incomplete. This ebook used to be created for doctors, scholars, and participants of most people who are looking to behavior scientific 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 Carnitine Palmitoyltransferase II Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Mitochondria, which are structures in each cell that convert molecules into energy, each contain a small amount of DNA. Because only egg cells contribute mitochondria to the developing embryo, only females can pass on mitochondrial conditions to their children. Mitochondrial disorders can appear in every generation of a family and can affect both males and females, but fathers do not pass mitochondrial traits to their children. Leber hereditary optic neuropathy (LHON) Help Me Understand Genetics 41 Many other disorders are caused by a combination of the effects of multiple genes or by interactions between genes and the environment.

This makes it difficult to determine a person’s risk of inheriting or passing on these disorders. Complex disorders are also difficult to study and treat because the specific factors that cause most of these disorders have not yet been identified. By 2010, however, researchers predict they will have found the major contributing genes for many common complex disorders. What Information about a Genetic Condition Can Statistics Provide? Statistical data can provide general information about how common a condition is, how many people have the condition, or how likely it is that a person will develop the condition.

What Is Uniparental Disomy? Uniparental disomy is a factor that influences how some genetic conditions are inherited. Uniparental disomy (UPD) occurs when a person receives two copies of a chromosome, or part of a chromosome, from one parent and no copies from the other parent. UPD can occur as a random event during the formation of egg or sperm cells or may happen in early fetal development. In many cases, UPD likely has no effect on health or development. Because most genes are not imprinted, it doesn’t matter if a person inherits both copies from one parent instead of one copy from each parent.

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