Progeria: Unveiling the Rarest Form of Premature Aging and Ongoing Research Efforts
Understanding Progeria Progeria, scientifically known as Hutchinson-Gilford Progeria Syndrome (HGPS), is a rare genetic condition that mirrors the signs of rapid aging in children. This premature aging disease affects roughly one in twenty million individuals worldwide. Recognizing and understanding this condition is vital for raising awareness and advancing research toward better management...
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