ALL YOU NEED TO KNOW ABOUT: LAFORA DISEASE

Lafora disease is a rare and serious genetic disorder that affects the brain and nervous system.

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It belongs to a group of conditions known as progressive myoclonic epilepsies. These diseases cause seizures, loss of motor skills, and mental decline

Lafora disease is a rare but serious disorder that significantly impacts the lives of those who have it. While there is currently no cure, research into potential treatments is ongoing. For now, managing the disease with medications, therapies, and supportive care is the best way to improve the quality of life for individuals with it, say studies.

Given its rarity, it’s important for both doctors and families to be aware of the signs and symptoms of Lafora disease. Early diagnosis can help with planning care and offering the right support, even though treatment options are limited. Here is all you need to know about Lafora disease:

What is Lafora disease?

Lafora disease is a rare and serious genetic disorder that affects the brain and nervous system. It belongs to a group of conditions known as progressive myoclonic epilepsies (PMEs). These diseases cause seizures, loss of motor skills, and mental decline. Lafora disease usually begins in adolescence, typically between the ages of 10 and 18, and worsens quickly, leading to a severe decline in quality of life. The disease is caused by the buildup of abnormal structures called Lafora bodies in the brain and other tissues, which interfere with normal brain function.

It is said that the disease derives its name from Spanish neuropathologist Gonzalo Rodríguez Lafora, who first documented it in an adolescent patient who was experiencing progressive myoclonic epilepsy.

What causes Lafora disease?