Hutchinson-Gilford Progeria Syndrome
Jul 02, 2026
Progeria Syndrome: The Rarest Case of Premature Ageing
Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS) and Benjamin button disease, is one of the rarest and most dramatic genetic disorders known to medicine. Characterized by rapid and premature ageing in children, this condition affects approximately 1 in 20 million people worldwide. Children with p...
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