Personalized Medicine Research Paper Example | Topics and Well Written Essays - 750 words

alter Medicine - Research Paper poserWith the simple blood test, disorders related to genes are detected. This was revealed in the regard by Holtzman and Shapiro (1998) where there was a substantial reduction in the birth of thalassaemia among high risk in Cyprus, Sardinia and in the Mediterranean regions. with prenatal diagnosis, couples are given the option for selective termination of pregnancy believed to carry genetic abnormalities. The study also found out that screening tests are helpful in determining other wellness problems such as sickle cell anemia, phenylketonuria, thyroid carcinoma, and multiple endocrine neoplasias that may arise as a result of defective gene combinations. Not only that physical abnormality could be limited yet also the psychological sequels as a result of discrimination are also prevented. With these breakthroughs in genetic science, modify medicine emerged in an effort to dissect the many combinations of genes to optimize preventative measures of patients to shrivel up the number of incidences. The technology employed in modern genetics also laid the foundation to experts bum the personalise medicine to include a more complex study such as cytogenetics, crab louse genetics, and cell biology in providing patients with individualized treatment. The individualized therapeutic care is based on the notion that patients do not respond to the same selected medication. The study of the patients protein including the genetic and metabolic compose helps in stratifying the disease. which is helpful in proper medication and dosage. In addition, modern genetic technology provided personalized medicine with the basics of going in depth studies of complex diseases such as cancer, diabetes, and heart diseases. This way, personalized medicine serves as the extension of traditional approach in understanding and treating disease. Benefits of personalized medicine Personalized medicine has varied benefits not only to individuals at ris k of possible genetic health problems but also to medical practitioners and to the p misemployaceutical companies as well. Individuals at risks can request diagnostic test at present from pharmaceutical companies for certain diseases without seeking the authorization of the physician. Companies such as 23ndMe Incorporated, decodeMe, and Navigenics provide services on genome profile to consumers. The service offered by these companies provides the public convenience and accessibility to the test for diagnosis. Furthermore, it promotes diagnostic awareness to the public in general (Haga, 2009). However, the same study warns that the non interference of a physician might lead to miscommunication leading to psychosocial harm and impacts life decision such as unnecessary family