Progeria Essay

Not many people in the world know the name of progeria. Progeria is a rare syndrome in children by physical signs and symptoms of premature age. The signs of progeria are noticed around the age of 18-24 months. Children with the disease usually die of heart disease at the age of 13, their lifespan is around 8-21 years. Since the Progeria Research Foundation that was created in 1999, they have discovered children with the disease in 40 countries. Research is still ongoing. The frequency of a child with progeria is one in four million newborns. 200-250 children in the world are living with progeria. The disease affects both male and female and all races. The inheritance of progeria is not on a sex chromosome and its dominant which means one copy of the gene in each cell is sufficient to cause progeria. Almost always occurs in people with no history of the disorder. The gene change is almost always a chance but is extremely rare. Chances with a child who already has progeria and it happening again is two-three percent. The increase is due to a condition called mosaicism, where a parent has the genetic mutation for the disease in their cells but does not have the …show more content…
Severe hardening of the arteries is a complication of this disease. The walls of your arteries blood vessels that carry your nutrients and oxygen from the heart to the rest od our body-stiffen and thicken, often restricting blood flow. Most children die from problems with blood vessels that supply the heart, resulting in heart attack and congestive heart failure. Problems with blood vessels that supply the brain, result in a stroke. Other health factors are arthritis, nearsightedness, and increased risk of