Progeria Syndrome (cont.)

Hutchinson-Gilford progeria syndrome is considered an autosomal dominant condition, which means one copy of the altered gene in each cell is sufficient to cause the disorder. The condition results from new mutations in the LMNA gene, and almost always occurs in people with no history of the disorder in their family.

Experience severe hardening of the arteries (arteriosclerosis) beginning in childhood. This condition greatly increases the chances having a stroke at a young age. These serious complications can worsen over time and are life-threatening for affected individuals.

These resources address the diagnosis or management of Hutchinson-Gilford progeria syndrome and may include treatment providers.

• Gene Review: Hutchinson-Gilford Progeria Syndrome
• Gene Tests: Progeroid Laminopathies

You might also find information on the diagnosis or management of Hutchinson-Gilford progeria syndrome in Educational resources and Patient support.

• To locate a healthcare provider, see How can I find a genetics professional in my area? in the Handbook.

Source: MedicineNet.com
http://www.medicinenet.com/progeria_syndrome/article.htm