Progeria Report Essay -- essays research papers fc

Genetics determine the traits an individual forget inherit from their p atomic number 18nts. In society today, the role of genetics is crucial they decide iodins physical coming into court as well as their personality. However, if there is a mutation rigid in one of the genes that a kid receives it is very likely a deformity will be present. A disused yet bleak defect from a gene mutation such as this is Progeria. This sickness is an untoward one that may occur in two forms, both Hutchison-Gilford Progeria or Werner syndrome. Not only do they affect the bone construction and appearance of the child, but they substantially shorten their life spans.      Hutchison-Gilford disorder was branch discovered and described by John Hutchison in 1886. However, in 1904 battle of Hastings Gilford named the disorder Progeria after doing some of his own research on it (Malady). around a year after Gilford presented his Progeria research, Otto Werner discovered a dis order by which he called "inaugural-dissertation". It was not until about 1935 that Oppenheimer and Kugel named innaugaral dissertation Werner Syndrome (Werner).      Progeria is a very rare disorder, affecting one out of eight million children in the Hutchison-Gilford form. Werner Syndrome is to a greater extent(prenominal) common yet still infrequent, affecting one out of one million children. Both types of Progeria affect specific ethnicities Hutchison-Gilford occurs most frequently in Caucasians, while Werner Syndrome affects mostly children of the Japanese and Sardinian background. This disorder is fatal in both cases, although the life span of one with Werner Syndrome, living to the age of approximately 46, is significantly longer then one with Hutchison-Gilford who will only hold out to the age of 13 (Werner).      Progeria is commonly referred to as "early aging distemper" however, this disorder has nothing to do wi th a child aging rapidly. The symptoms of Progeria in both Hutchison-Gilford and Werner are very similar and they do appear to speed the aging process. A child with Hutchison-Gilford has an entirely bald head and face. Their scalp, veins and look are clearly more prominent then a child without this disorder. The childs jaw will appear small and many times, he will be toothless, for Progeria causes delayed tooth formation. In addition, a child will ... ... Werner is more common, but much less well known (Kugler).      Progeria is a fatal, unfortunate disease. The fact that deformed children are completely mentally fit, and know they are different is terrible. It mustiness be hard to handle stares, smirks, pointing fingers, and still start to cope with the fact that you will probably not live recent fifteen years old. The public needs to be more meliorate on this disease, and not treat it as so much of a sick deformation. Infected children may look different , but they are the akin as anyone else. There are many organizations around that are aggregation money for the furthering of research, and to educate the public.     I could never imagine being the enkindle who has to make a choice of having a possibly mutated baby. Even with the odds in your favor, imagine choosing to have a baby, than discovering he will be born infected and you will outlive your son. Making that choice must be incomprehensivly difficult for both parents involved. Progeria is a mutation that needs to be dealt with very soon. Works CitedMalady of the Month-Progeria. Kugler, Mary. Progeria Syndroms. Werner Syndrome.