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Friday, March 22, 2019

Clinical Genetic Disorder: Beta Thalassemia Essay -- Genetic Blood Dis

tail and his wife bloody shame decided that after 3 years of marriage it was time for them to bring a child into their life. tin can and bloody shame lived on the coast of Italy, where the weather was always sunny and strong and the water not but a stone toss away. John and Mary decided that it was the right time, then, 9 months later they conceived a son, they named him heat content. During the introductory two years of Henrys life John and Mary noticed abnormalities in Henrys development. Henry did not encourage weight or grow as he was expected to. He also exhibited signs of weakness and fatigue. Henry had always been pale, and this alone was never teeming to alarm suspicion but Henrys paleness started to put forward to a more yellowish tint, and along with these other signs raised plenteous suspicion to take Henry to the hospital. The doctor took blood from Henry to be tested. After the test result came back the doctor concluded that Henry had an enlarged spleen and live r. He was suffering from a he bolshieitary unhealthiness called beta-thalassemia.John and Mary in complete dismay questioned the doctor as to how their son suffered from a hereditary disease that neither of them suffered from. The doctor certified the grieving parents that both of them must be carriers of the mutated HBB gene. During the conception of Henry, John and Mary must have passed on the mutated recessive gene on olibanum with the presence of two mutated recessive HBB genes caused Henry to develop Beta-thalassemia. The doctor move to explain that the beta-thalassemia causes the beta-globin, a subunit of hemoglobin, to not be produced creating non-functional hemoglobin. Without sufficient hemoglobin, red blood cells do not develop properly, causing a shortage of mature red blood cells. This lack of red bl... ....MedicineNet, Beta thalassaemia (A Genetic Blood Disorder). Accessed January 27, 2014.http//www.virtualmedicalcentre.com/diseases/thalassaemia-mediterranean-anem ia-cooley.Palit, Sarmi, Robiul Bhuiyan, Aklima Jannatul, Raju Dash, and Talha Emran. Journal of Basic and Clinical Pharmacy, A playing field of the prevalence of thalassemia and its correlation with liver function test in different age and sex group in the Chittagong district of Bangladesh . utmost(a) modify December 31, 2012. Accessed January 30, 2014. http//www.jbclinpharm.org/article.asp?issn=0976-0105year=2012volume=3issue=4spage=352epage=357aulast=Palit.Virtual Medical Centre, Thalassaemia (Mediterranean anemia Cooleys anemia). Last modified 11 2, 2008. Accessed January 27, 2014.http//www.virtualmedicalcentre.com/diseases/thalassaemia-mediterranean-anemia-cooleys-anemia/130

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