Lafora Disease: Understanding a Rare Genetic Disorder
What is Lafora Disease?
Lafora Disease is a rare, inherited form of epilepsy characterized by the presence of abnormal glycogen deposits known as Lafora bodies in various tissues, particularly in the brain. This progressive neurological disorder typically manifests in late childhood or early adolescence, leading to severe seizures, cognitive decline, and ultimately, a significant reduction in quality of life.
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