Hutchinson-Gilford progeria syndromeis a genetic condition characterized by the dramatic, rapid appearance of aging beginning in childhood. Affected children typically look normal at birth and in early infancy, but then grow more slowly than other children and do not gain weight at the expected rate (failure to thrive). They develop a characteristic facial appearance including prominent eyes, a thin nose with a beaked tip, thin lips, a small chin, and protruding ears. Hutchinson-Gilford progeria
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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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