Progeria is one of the strange disease that enrich the world, according to the study of disease, progeria disease caused by a small error in the genetic code of the child, but to destroy and change someone’s life. the average child will be born with this disease, at the age of 13 years die because their bodies faster than baldness, heart disease and aging, weakening of the bones and joints. Fortunately disease Progeria is extremely rare, only about 48 people suffer from this disease worldwide, but there is a family of 5 children about this disease
Progeria is certainly a rare inherited disorder, as a rapidly aging are seen from childhood. Simply put, it is normal for older people, but children. It is three times the pace can be as Hutchinson-Gilford disease. the majority of adolescents with progeria suffering from a mutation, or the natural probability of the gene encoding an essential protein each lamination.
Progeria, as being a rare disease, only has concerning 40-45 identified conditions in the world. This complaint cannot be influenced by the parents for their children due to the fact children usually accredited to remain for a certain duration adolescents. a family in India has a number of children would suffer from this disease, and two seem to be dead.
Whose suffer this disease, have a fast life. Special circumstances, people within 30 years. Solutions are only capable of problems such as cardiovascular disease, to reduce, prevent, or may be a functioning heart low doses of drugs. a high-calorie diet can probably extend the life. There is a growth hormone treatment analyzed to learn if the cure progeria.