Mixed Hyperlipidemia : Causes

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Causes could include:
Familial combined hyperlipidemia is the most common disorder of increased blood fats that causes early heart attacks. It is genetic, which means it is caused by a problem with your genes. However, researcher have yet not identified the specific ge...
Source:ADAM
Date:January 23, 2008
Conditions with a link to the individual ' s genetic make-up. Genetic disorders are conditions that can be traced to an individual ' s heredity.
Source:Gale Encyclopedia of Childhood and Adolescence
Detailed information on the different types of genetic diseases that can affect a pregnancy
Source:StayWell
Detailed information on the most common congenital and hereditary disorders in children
Source:StayWell
A Harvard Medical School physician answers your question about the hereditary elements of addiction.
Source:StayWell
Any unusual variation or abnormality in the shape, structure, and/or function of an organ, body part, or tissue is commonly referred to as a birth defect. However, congenital anomaly is the more accurate and preferred term, since birth defect can be misinterpreted to mean a defect produced by the birthing process.
Source:Gale Encyclopedia of Genetic Disorders Part II
Variations within the DNA sequence of a particular gene affect its function, and may cause or predispose an individual a particular disease. Alterations in the genome may increase the frequency of disorder and disease with entire populations.
Source:Gale Encyclopedia of Genetic Disorders Part II
The traditional method used to study an inherited disease is to observe the pattern of its distribution in families through examination of a pedigree, the construction of which begins with the individual first known to have the disease. The pedigree pattern allows one to judge whether or not the distribution conforms to Mendelian principles of segregation and assortment, and thus represents single-factor inheritance.
Source:Gale Encyclopedia of Public Health
Variations within the DNA sequence of a particular gene affect its function and may cause or predispose an individual a particular disease. Alterations in the genome may increase the frequency of disorder and disease with entire populations.
Source:Gale Encyclopedia of Genetic Disorders Part I
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