Progeria (Hutchinson-Gilford syndrome)

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Progeria

Alternate Names : Hutchinson-Gilford syndrome

Definition

Progeria is a disease that produces rapid aging, beginning in childhood.

Overview, Causes, & Risk Factors

Progeria is a rare condition that is remarkable because its symptoms strongly resemble normal human aging, but occur in young children.

Ninety percent of children with progeria have a mutation on the gene that encodes the protein lamin A. Progeria usually occurs without cause. It is only very rarely seen in more than one child in a family.

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Coronary artery blockage

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Progeria : Definition
Progeria : Overview, Causes, & Risk Factors
Progeria : Symptoms & Signs
Progeria : Diagnosis & Tests
Progeria : Treatment
Progeria : Support Groups
Progeria : Prognosis (Expectations)
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Coronary artery blockage

Review Date : 8/26/2009
Reviewed By : Chad Haldeman-Englert, MD, Wake Forest University School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

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