Progeria, also known as Hutchinson-Gilford progeria syndrome, is a rare genetic condition that causes rapid aging in children, leading to features like wrinkled skin, hair loss, and a small face relative to head size. This condition is caused by a mutation in the LMNA gene and typically results in severe cardiovascular issues, with an average life expectancy of around 15 years.#followers #followerseveryonehighlights #followerseveryonehighlightseveryone | Frema Shows TV
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Answered: You are a researcher working on a treatment for Hutchinson-Gilford progeria syndrome, an extremely rare genetic disorder that causes accelerated aging in… | bartleby
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Dr Kailasam on Instagram: "Progeria Explained: The Rare Genetic Disorder That Ages Kids Fast Progeria, also known as Hutchinson–Gilford Progeria Syndrome (HGPS), is a rare genetic disorder caused by a mutation in the LMNA gene. It makes children age rapidly, leading to thin skin, hair loss, stiff joints, and early heart disease — while their intelligence remains normal. Learn the causes, symptoms, and facts about this fascinating syndrome in under 10 seconds. #Progeria #HGPS #RareGeneticDisorder
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Uni Medical care on Instagram: "🧬 Progeria, or Hutchinson-Gilford syndrome, is a very rare genetic disorder that causes children to show signs of premature aging 👶➡️👴, usually after the first two years of life. ⚠️ This disease leads to accelerated aging and often causes death from complications such as heart disease ❤️‍🩹 or strokes 🧠💥 before reaching late adolescence or early twenties. 🔍 Main Symptoms - 🐢 Slowed growth - 🧊 L
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