P rogeria, also known as Hutchinson-Gilford progeria syndrome, is a rare disorder that profoundly reshapes the lives of those ...

Hutchinson-Gilford Progeria Syndrome. HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus. In HGPS patients, the cell nucleus has ...

Progeria, also known as Hutchinson-Gilford Progeria Syndrome, is an extremely rare genetic disorder, characterised by accelerated ageing in children.

The US teenager was diagnosed with Hutchinson-Gilford progeria, also known as Benjamin Button disease, when she was three months old. It's a rare fatal condition which causes problems with growth ...