Hutchinson-Gilford progeria syndrome; HGPS
Progeria is a rare genetic condition that produces rapid aging in children.
Progeria is a rare condition. It is remarkable because its symptoms strongly resemble normal human aging, but it occurs in young children. In most cases, it is not passed down through families. It is rarely seen in more than one child in a family.
The health care provider will perform a physical exam and order laboratory tests. This may show:
Cardiac stress testing may reveal signs of early atherosclerosis of blood vessels.
Genetic testing can detect changes in the gene (LMNA) that causes progeria.
There is no specific treatment for progeria. Aspirin and statin medicines may be used to protect against a heart attack or stroke.
Progeria Research Foundation, Inc. -- www.progeriaresearch.org
Progeria causes early death. People with the condition most often only live to their teenage years (average lifespan of 14 years). However, some can live into their early 20s. The cause of death is very often related to the heart or a stroke.
Complications may include:
Contact your provider if your child does not appear to be growing or developing normally.
Gordon LB. Hutchinson-Gilford progeria syndrome (progeria). In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics. 21st ed. Philadelphia, PA: Elsevier; 2020:chap 109.
Gordon LB, Brown WT, Collins FS, et al. Hutchinson-Gilford progeria syndrome. GeneReviews. 2015:1. PMID: 20301300 pubmed.ncbi.nlm.nih.gov/20301300/. Updated January 17, 2019. November 1, 2021.BACK TO TOP
Review Date: 7/30/2021
Reviewed By: Anna C. Edens Hurst, MD, MS, Associate Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
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