Hutchinson-Gilford Syndrome: Treatments

Treatment for Hutchinson-Gilford Syndrome (HGS) is generally aimed at mitigating symptoms of the disease. There is no cure. Treatment begins with a diagnosis, which can be obtained with a free genetic test from the Progeria Research Foundation. Such a test sequences the relevant gene, and searches for the mutation that typifies HGS. After a positive diagnosis, a number of treatments may be used to prolong the life of an HGS child.

Frequently, the most important treatment of HGS is an aspirin or blood-thinning regimen designed to prevent the heart problems that usually are responsible for death in HGS children. A number of medications may be used for this purpose. Usually dietary changes are also necessary, both for heart health and in order to maintain body fat, another problem for HGS patients. A regimen of physical therapy is recommended, to moderate the frequent atrophy of muscles that accompanies the disease.