Progeria
Also called: Hutchinson-Gilford progeria syndrome
A progressive genetic disorder that causes children to age rapidly.
- Requires a medical diagnosis
- Lab tests or imaging always required
- Chronic: can last for years or be lifelong
The genetic mutation occurs randomly and isn't inherited.
Extremely rare: Fewer than 500 cases per year (Nigeria)
Consult a doctor for medical advice
Sources: College of Medicine, University of Ibadan and others. Learn more
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2 May 2023 · This genetic disorder is extremely rare and progressive. It causes children to age rapidly, beginning in their first two years of life.
5 Sept 2022 · WebMD explains progeria, a rare genetic condition that causes a child's body to grow old quickly. There's no cure, but treatment can ease or ...
7 Dec 2022 · Progeria is a rare genetic condition that causes rapid aging in children. A tiny genetic mutation causes the disease, which is always fatal.
Progeria is a specific type of progeroid syndrome, also known as Hutchinson–Gilford syndrome or Hutchinson–Gilford progeroid syndrome (HGPS).
5 Apr 2024 · Progeria, any of several rare human disorders associated with premature aging. The two major types of progeria are Hutchinson-Gilford ...
2 May 2023 · This genetic disorder is extremely rare and progressive. It causes children to age rapidly, beginning in their first two years of life.
The disease is characterized by definite defects in nuclear shape due to the mutated gene resulting in distorted nuclear membranes in 50 per cent of the cells ...
1 May 2016 · Hutchinson-Gilford progeria syndrome is a genetic condition characterized by the dramatic, rapid appearance of aging beginning in childhood.
Progeria, or Hutchinson-Gilford progeria syndrome (HGPS), is a rare, fatal, genetic condition of childhood with striking features resembling premature aging.
Progeria. HGPS is a rare genetic disorder that results in a short life span with characteristics of rapid aging, with death typically resulting from ...