Hutchinson-gilford progeria syndrome

Overview

What is Hutchinson-Gilford Progeria syndrome?

Hutchinson-Gilford Progeria syndrome, or progeria, is a rare genetic condition that makes a person's body seem to age much faster than expected. Children with progeria have trouble growing and gaining weight. Children typically experience medical issues that are usually associated with older age, such as hair loss, bone changes, hearing loss, joint stiffness, atherosclerosis (hardening of the arteries), and heart disease. As of June 14, 2016, there is no cure for progeria, but the symptoms and medical issues can be monitored and treated to increase a child's quality of life.

SOURCE: Emory University - Department of Human Genetics in collaboration with ThinkGenetic • https://www.thinkgenetic.com/diseases/hutchinson-gilford-progeria-syndrome/overview/6094 • DATE UPDATED: 2016-06-15

References

Progeria Research Foundation's "The Progeria Handbook"

Gordon LB, Brown WT, Collins FS. Hutchinson-Gilford Progeria Syndrome. 2003 Dec 12 [Updated 2015 Jan 8]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1121/

This content comes from a hidden element on this page.

The inline option preserves bound JavaScript events and changes, and it puts the content back where it came from when it is closed.

Remember Me