Introduction and Causes of New Rare Diseases
The discovery of new rare diseases is driven by advances in genetic research, better diagnostic tools, and the identification of previously unrecognized conditions. Many rare diseases have genetic origins, often resulting from mutations, chromosomal abnormalities, or inherited patterns. Environmental factors, such as exposure to toxins or infections, can also contribute to the emergence of rare conditions. Understanding the root causes helps in developing targeted therapies and improving diagnostic accuracy. Continuous research and collaboration among scientists, geneticists, and clinicians are essential for uncovering the mysteries behind these diseases and advancing patient care.
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