Progeria Children's

Progeria infantum, also known as progeria infantium, is a rare genetic disease that is characterized by premature aging in childhood. This condition occurs due to a mutation in the LMNA gene, which codes for the protein lamin A, an important component of the nuclear envelope of cells.

Children with progeria are born normal, but by the age of two they begin to show signs of aging, such as hair loss, skin becoming thinner and less elastic. They also often have vision, hearing and heart problems. On average, children with progeria live up to 14 years.

Progeria childhood is a rare condition occurring in approximately one child in 8 million births. The cause of the LMNA gene mutation is unknown, and there is currently no cure for childhood progeria. However, there are treatments that help improve the quality of life of children with progeria, such as growth hormone therapy and treatment for heart problems.

In addition, research into genetics and cell biology continues, with hopes that in the future new treatments and perhaps even ways to prevent this rare disease will be found.

Progeria in childhood is a tragic condition that limits the life path of children and their opportunities. However, through scientific and medical research, there is hope that we can help children with progeria and improve their quality of life.