People diagnosed with this disorder usually have small, fragile bodies, like those of older adults. The head is usually large relative to the body, with a narrow, wrinkled face and a beak nose. Prominent …

May 2, 2023 · 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 …

Dec 7, 2022 · 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 …

Dec 31, 2025 · 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 (HGPS, often called just “progeria”) is a rare genetic condition in which children show signs of early aging due to mutations in the LMNA gene. It affects multiple …

Dec 27, 2013 · 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 …

Dec 12, 2003 · The clinical diagnosis of Hutchinson-Gilford progeria syndrome (HGPS) can be established in a proband when characteristic pathognomonic features emerge. Molecular testing …

Jan 10, 2026 · progeria, any of several rare human disorders associated with premature aging. The two major types of progeria are Hutchinson-Gilford progeria syndrome (HGPS), which has its onset in …

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 …

Oct 28, 2025 · What is progeria? Progeria is an extremely rare genetic disorder that causes rapid aging in children and severe failure-to-thrive. Children with progeria often appear healthy at birth but begin …