Progeria: Insights into a Rare Genetic Disorder

Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS), is a rare genetic disorder characterized by accelerated aging in children. Here are some key details about the condition:

Symptoms

Children with Hutchinson-Gilford Progeria Syndrome (HGPS) exhibit a range of symptoms that mimic accelerated aging. Here’s a detailed overview of the typical symptoms associated with the condition: read more

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