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Monday, February 18, 2019

Essay --

bizarre contagious disease that seems to accelerate ageing could hold the key to longer lives for children with progeria.Progeria is an exceedingly rare, fatal genetic condition which causes babies to age quickly. Progeria was first described in an academic journal by Dr. Jonathan Hutchinson in 1886 and also by Dr. Hasting Gilford in 1897 both man was from England (Nordqvist 1). After discovering the two people they later came up with a new name for Progeria called Hutchinson-Gilford Progeria Syndrome (HGPS). Today in life thither 53 cases of Progeria around the world and only 2 in the UK.1 in e really 4 to 8 million babies are born with Progeria. Progeria issuance all race equal boys and girls. As newborn, children with Progeria usually appear natural at birth. However, within a year their growth rate slows and they before long are much smaller and weigh less than other children they age. and so later they begin to accelerate aging and some signs of progeria may start. crop failure, Loss of body, Loss of hair, Skin starts to look aged, Stiffness in the joint, rosehip dislocation, Generalized atherosclerosis, and stroke are all symptoms that child with Progeria will have. Children who nonplus from Progeria are genetically susceptible to premature, progressive heart disease (Davis 2). Progeria appears to number without cause and it is non seen in siblings of affected children. Children with Progeria have a astonishingly appearance. 90% of children with Progeria have a mutation on the gene that encodes Lamin A, a protein that holds the nucleus of the cell together (Conley 4). Lamin A protein pisss the nucleus stable it leads to the cover of premature aging among Progeria patients. Experts do not believe that Progeria is hereditary. In close 1 in ev... ...yday because you they never know when they might lose them. Progeria is not usually passed down in family. Children with Progeria often suffer from symptoms typically seen in elderly people (Da vis1). People inherit the disease only one and only(a) copy of the LMNA gene is enough to cause the disease because it is an autosomal prevailing gene. The Progeria Research Foundation was created in 1999. Progeria does have parallels with normal ageing at least in one key aspect how out origin vessels deteriorate. Researchers found that a drug known as rapamyein slowed and even halt the disease progression the cells. Progeria only affected newborn babies. Progeria is a very rare disease that no one knows where it comes from. Research today is pacify havent come up with a way to interrupt the cure for Progeria. Some research found a way to make Progeria patients live longer then the age 13.

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