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Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford progeria syndrome, is an extremely rare, progressive genetic disorder. It causes children to age rapidly, starting in their first two years of life.
Progeria is a specific type of progeroid syndrome, also known as Hutchinson–Gilford syndrome or Hutchinson–Gilford progeroid syndrome (HGPS). [8] A single gene mutation is responsible for causing progeria. The affected gene, known as lamin A (LMNA), makes a protein necessary for holding the cell nucleus together.
Progeria is an extremely rare genetic disease that causes rapid aging in children. Newborns with the disorder appear to be healthy at birth but usually start to show signs of premature aging during their first one to two years of life.
Current research seeks to understand progeria and identify new treatment options. Some areas of research include: Studying genes and the course of the condition to understand how it progresses. This may help identify new treatments. Studying ways to prevent heart and blood vessel disease.
Progeria is also known as Hutchinson-Gilford progeria syndrome (HGPS) or the “Benjamin Button” disease (named after the short story and movie ‘The Curious Case of Benjamin Button’). It’s a...
Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging. The condition, which derives its name from "geras," the Greek word for old age, is estimated to affect one in 4 million newborns worldwide.
Progeria syndrome is a group of disorders that cause rapid aging in children. Learn more about this rare and fatal condition.
What is Progeria? Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS), is a rare, fatal genetic condition of “rapid-aging” in children.
Hutchinson-Gilford progeria syndrome is a genetic condition characterized by the dramatic, rapid appearance of aging beginning in childhood. Affected children typically look normal at birth and in early infancy, but then grow more slowly than other children and do not gain weight at the expected rate (failure to thrive).
Classic and nonclassic genotype Hutchinson-Gilford progeria syndrome (HGPS) are characterized by clinical features that develop in childhood and resemble some features of accelerated aging. Children with progeria usually appear normal at birth and in early infancy.