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rare genetic disorder causing rapid aging in children

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic disorder characterized by rapid aging in children, typically becoming apparent within the first two years of life. It is caused by a mutation in the LMNA gene, which leads to the production of an abnormal protein called progerin, resulting in cellular instability and the accelerated aging process.

Related Terms

• Progerin
• Gorlin Syndrome
• Hereditary Hypotrichosis Simplex
• Lipoid Proteinosis
• Woodhouse-Sakati syndrome
• PAPA Syndrome
• Birt–Hogg–Dubé syndrome
• Cronkhite-Canada Syndrome