Category: Genetic Disorders / Premature Aging Syndrome
Progeria, specifically Hutchinson-Gilford Progeria Syndrome (HGPS), is an extremely rare, fatal genetic condition characterized by dramatic, rapid aging in children, leading to an average lifespan of 14.5 years.
Approximately 1 in 4 to 8 million live births (Source: Progeria Research Foundation)
Discover the latest clinical trials and treatments for Progeria on JourneyForHealth.
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