Tag: Rare Conditions

Read more Progeria, also known scientifically as Hutchinson-Gilford Progeria Syndrome (HGPS), is an extraordinarily rare genetic condition that affects approximately 1 in every 4 to 8 million newborns. This syndrome is characterized by accelerated aging in children, with the most prevalent form being Hutchinson-Gilford Progeria. What Are the Symptoms of Progeria? Children diagnosed with progeria…