Mother Discovers Gene Mutation Responsible for Son's Progeria
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Mother Discovers Gene Mutation Responsible for Son's Progeria
Oct 21, 2013
ABC News
Charlotte, who is deaf, has a genetic mutation known as Progeria, which causes her to age rapidly. Due to her condition, her age is eight times faster than usual aging, resulting in her looking much older than she should. Filmed and edited by Melisa Ozerska - a deaf young traveller Sorenson #DeafLifeStory | Seek the World
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Charlotte, who is deaf, has a genetic mutation known as Progeria, whic…
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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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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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