Hutchinson-Gilford progeria syndrome is a condition that manifests in rapid aging in children, often leading to premature osteoporosis and fragile bones. With only one in every four million babies ...

Hutchinson-Gilford syndrome (HGPS) is a rare and progressive disorder that causes children to age prematurely, often with an onset within the first few years of their life. This disorder is passed ...

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic disorder characterized by accelerated aging in children. This condition is caused by mutations in the lamin A gene, leading to the ...

She was 19 years old. Diagnosed at seven months old with Progeria — also known as Hutchinson-Gilford progeria syndrome — Beandri was not expected to live past the age of 14, as her condition ...