Hutchinson-Gilford Progeria Syndrome: From Genetic Mutation to Patient Care
Imagine a child who looks and feels healthy at birth, only to begin aging decades ahead of schedule before their second birthday. That’s the reality for children born with Hutchinson-Gilford Progeria Syndrome (HGPS), more commonly called Progeria. It’s an incredibly rare condition, showing up in roughly one out of every four to eight million births,…
