Medical genomic can be defined as the utilization of genome-based information in the making of clinical decisions. A broader concept, personalized medicine, is often used to describe the models of healthcare that emphasize the application of an individual’s unique environmental, genomic, genetic, and clinical information to the treatment and prevention of diseases (Brunicardi; Offit). In their practice, doctors combine the results of patient data, which include individual genomic information, family history, medical history, conventional test results, and symptoms. The combination of the data allows the physicians to diagnose diseases accurately and personalize treatment strategies (Alzu’bi et al.). ...
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Medical genetics is viewed as one of the ways to diagnose and manage any hereditary disorders. It encompasses various areas, such as physician’s clinical practice, activities in diagnostic laboratory, and even research to point out the possible causes of genetic disorders. This medical approach can be beneficial many people, as there could be new ways to predict any future diseases that may arise due to the disorders of the gene. It can also benefit the children when it comes to knowing the possibility of having medical issues based upon the tested genes of his or her parents. However, ...
The condition is described as the embryonic forebrain and the faces of human babies. The etiology is heterogeneous genetically and therefore is passed from parents to offsprings. It may also have some environmental inclination (Mallick et al, 2014, para 1). HPE is subdivided into four classes ranging from the least to the most severe kind (Nanni, Schelper & Muenke, 2010, para 2). The brain is bifurcated into two hemispheres. Only 3% of the fetuses develop to delivery. Two-thirds of the affected develop alobar HPE. Which is the most severe of them. The prevalence of the condition has been quoted as ...
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ORDER AN ESSAYLis Rodriguez
Lab 1 ASA College Abstract Patau’s syndrome is a rare genetic disorder that involves trisomy 13. The condition is characterised by either an extra copy of the autosomal chromosome number 13 or a translocation to chromosome 13 from another chromosome. There are severe symptoms observed in the unborn and newborn children having this defect. Polydactyly, cleft lips, physical retardation, mental retardation, heart defects are few of the many symptoms. The disease can be diagnosed during gestation via screening methods followed by several analytical procedures like FISH, karyotyping and microarray on samples of blood and serum from the pregnant ...
