Progeria - Symptoms and causes - Mayo Clinic
2023年5月2日 · 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. Children with progeria generally appear healthy at birth.
Progeria - Wikipedia
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 (Hutchinson-Gilford Progeria Syndrome — HGPS): …
2022年12月7日 · 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. Their growth rate slows and they don’t gain weight as expected.
About Progeria - National Human Genome Research Institute
2013年12月27日 · 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: Types, Symptoms, Treatment, Prognosis - Verywell Health
2022年12月8日 · Progeria is a condition in which an affected individual experiences rapid or early aging. There are two main types of progeria; one form is diagnosed in infancy or early childhood, and the other is diagnosed in adolescence or early adulthood.
Progeria: Causes, Symptoms, and Treatments - WebMD
2022年9月5日 · 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 - Diagnosis and treatment - Mayo Clinic
2023年5月2日 · Diagnosis. Health care providers may suspect progeria based on symptoms. A genetic test for changes in the LMNA gene can confirm the diagnosis of progeria. A thorough physical exam of your child includes: Measuring height and weight. Putting measurements on a growth curve chart.
Progeria: What Is It, Causes - Osmosis
2023年8月2日 · Hutchinson-Gilford Progeria Syndrome (HGPS) is an exceedingly rare disorder caused by a genetic mutation in the LMNA gene, leading to an abnormal form of the Lamin A protein called progerin. It is characterized by premature aging, failure-to-thrive, typical skeletal and facial features, and numerous abnormalities in various organ systems.
Progeria Syndrome - Healthline
2017年9月29日 · What is progeria syndrome? Progeria syndrome is the term for a group of disorders that cause rapid aging in children. In Greek, “progeria” means prematurely old.
Hutchinson-Gilford progeria syndrome - MedlinePlus
Hutchinson-Gilford progeria syndrome is a genetic condition characterized by the dramatic, rapid appearance of aging beginning in childhood. Explore symptoms, inheritance, genetics of this condition.