RGUHS Nat. J. Pub. Heal. Sci Vol No: 16 Issue No: 3 pISSN:
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“ We are the facilitators of our own creative evolution.”
- Bill Hicks
Genomic medicine has the potential to bring about a significant revolution in healthcare, particularly in the diagnosis of rare diseases. Genomic sequencing allows for a comprehensive analysis of an individual’s genetic makeup and uncovers the underlying genetic causes of certain conditions, leading to more accurate and timely diagnosis. Analyzing an individual’s genetic information provides risk stratification. Personalized treatments can potentially increase the effectiveness of interventions while minimizing adverse effects. The concept of precision medicine involves tailoring medical decisions and interventions according to the individual characteristics of each patient. This approach can lead to more successful outcomes by avoiding one-size-fits all treatments and instead focusing on therapies that are most likely to work for a specific patient. Genomic data provide insights into the likely progression of a disease, and prognosis prediction helping healthcare providers make informed predictions about the course of an illness and plan appropriate interventions.
Genomic information also contributes to the development of new drugs. By understanding the genetic basis of diseases, researchers can identify potential drug targets and design medications that specifically address the underlying molecular mechanisms of the condition. Genomic medicine generates numerous amounts of data that contribute to ongoing research efforts. Aggregated genomic data help researchers better understand the genetic basis of various diseases, leading to improved diagnostic methods and treatment strategies over time.
The potential of genomic medicine to revolutionize healthcare is promising, offering the hope of more precise and effective treatments for individuals with rare diseases, ultimately improving their quality of life and prognosis.
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