Multifactorial disease: Difference between revisions
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Revision as of 22:43, 10 February 2025
Multifactorial disease refers to any disease or disorder that is caused by a combination of genetic and environmental factors. These diseases are also known as complex or polygenic diseases.
Overview
Multifactorial diseases are not inherited in a simple Mendelian fashion. Instead, they are caused by multiple genes interacting with each other and with environmental factors. Examples of multifactorial diseases include heart disease, diabetes, hypertension, cancer, and obesity.
Genetic Factors
The genetic factors involved in multifactorial diseases are often difficult to identify because they do not follow simple inheritance patterns. Instead, they involve multiple genes that each contribute a small amount to the overall risk of developing the disease. These genes are often referred to as susceptibility genes.
Environmental Factors
Environmental factors that can contribute to the development of multifactorial diseases include diet, exercise, exposure to toxins, and lifestyle choices such as smoking and alcohol consumption. These factors can interact with genetic factors to increase or decrease the risk of developing the disease.
Diagnosis and Treatment
Diagnosis of multifactorial diseases often involves genetic testing to identify susceptibility genes, as well as assessment of environmental risk factors. Treatment typically involves managing symptoms and reducing environmental risk factors. In some cases, genetic counseling may be recommended for individuals with a family history of a multifactorial disease.
Research
Research into multifactorial diseases is ongoing and aims to identify the specific genes and environmental factors involved, as well as how they interact. This research could lead to new treatments and prevention strategies.
See Also

