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Revision as of 18:30, 10 February 2025
Genetic Disease
A genetic disease is a type of disease that is caused by an abnormality in an individual's genome. This abnormality can range from minuscule to major - from a discrete mutation in a single base in the DNA of a single gene to a gross chromosome abnormality involving the addition or subtraction of an entire chromosome or set of chromosomes.
Causes
Most genetic diseases are the direct result of a mutation in one gene. However, one of the most difficult problems ahead is to further elucidate how genes contribute to diseases that have a complex pattern of inheritance, such as in the cases of diabetes, asthma, cancer and mental illness. These diseases are multifactorial inheritance disorders, meaning they are caused by a combination of small variations in genes, often in concert with environmental factors.
Types of Genetic Diseases
Genetic diseases can be grouped into three main categories:
- Monogenic diseases: These are caused by a mutation in a single gene. Examples include cystic fibrosis, sickle cell anemia, and Marfan syndrome.
- Chromosomal diseases: These are caused by abnormalities in chromosomes, or by mutations in genes on the chromosomes. Examples include Down syndrome, Turner syndrome, and Klinefelter syndrome.
- Complex diseases: These are caused by a combination of genetic and environmental factors. Examples include heart disease, diabetes, and cancer.
Diagnosis and Treatment
The diagnosis of genetic diseases can be complex, often involving a combination of genetic testing, medical imaging, and physical examination. Treatment can vary widely depending on the specific disease, and may include gene therapy, medication, surgery, or physical therapy.
See Also
References
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