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

tooshie and his wife Mary decided that afterwards 3 years of marriage it was time for them to bring a electric razor into their life. bath and Mary lived on the coast of Italy, where the weather was always brave and warm and the water non but a stone jail 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 first two years of Henrys life John and Mary noticed abnormalities in Henrys development. Henry did not gain weight or grow as he was pass judgment to. He also exhibited signs of weakness and fatigue. Henry had always been pale, and this alone was never enough to alarm suspicion but Henrys luridness started to shift to a more yellowish tint, and along with these other signs embossed enough suspicion to take Henry to the hospital. The pay back took blood from Henry to be runneled. After the test result came back the set up think that Henry had an enlarged spleen and liver. He was su ffering from a familial disease called beta-thalassemia.John and Mary in complete dismay questioned the revivify as to how their son suffered from a hereditary disease that neither of them suffered from. The doctor informed 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 thus with the presence of two mutated recessive HBB genes caused Henry to develop beta-thalassemia. The doctor continued to explain that the beta-thalassemia causes the beta-globin, a subunit of hemoglobin, to not be produced creating non-functional hemoglobin. Without fit hemoglobin, red blood cells do not develop properly, causing a shortage of mature red blood cells. This lack of red bl... ....MedicineNet, Beta Thalassemia (A Genetic Blood Disorder). Accessed January 27, 2014.http//www.virtualmedicalcentre.com/diseases/thalassaemia-mediterranean-anemia-cooley.Palit, Sarmi, Robiul Bh uiyan, Aklima Jannatul, Raju Dash, and Talha Emran. Journal of Basic and Clinical Pharmacy, A study of the prevalence of thalassemia and its correlation with liver function test in different age and sex group in the Chittagong regularize of Bangladesh . operate modified December 31, 2012. Accessed January 30, 2014. http//www.jbclinpharm.org/article.asp?issn=0976-0105year=2012volume=3 fuck=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