Krabbe Disease is a rare, inherited disorder that affects the nervous system. It is also known as globoid cell leukodystrophy and is caused by a deficiency of the enzyme galactocerebrosidase. The disease is named after the Danish neurologist Knud Krabbe, who first described the condition in 1916.
There are two forms of Krabbe Disease: early-onset (infantile) and late-onset (juvenile or adult). The infantile form is the most common and severe type, with symptoms appearing within the first six months of life. The juvenile and adult forms are less common and typically have a more gradual onset and slower progression.
The symptoms of Krabbe Disease can vary depending on the age of onset and severity of the condition. In the infantile form, symptoms may include:
In the late-onset form, symptoms may include:
Krabbe Disease is caused by a mutation in the GALC gene, which provides instructions for making the galactocerebrosidase enzyme. Without this enzyme, toxic substances accumulate in the nervous system and cause damage to the myelin sheath that surrounds and protects nerve fibers. This results in the symptoms of Krabbe Disease.
Krabbe Disease is inherited in an autosomal recessive pattern, which means that a person must inherit two copies of the mutated gene (one from each parent) to develop the condition. If both parents carry one copy of the mutated gene, there is a 25% chance with each pregnancy that their child will inherit two copies and develop Krabbe Disease.
Krabbe Disease is a rare and devastating disorder that affects the nervous system. The symptoms and severity of the condition can vary depending on the age of onset and progression of the disease. While there is no cure for Krabbe Disease, early diagnosis and management of symptoms can improve the quality of
Krabbe disease, also known as globoid cell leukodystrophy, is a rare and progressive disorder that affects the nervous system. It is caused by a deficiency of an essential enzyme called galactocerebrosidase, which is responsible for breaking down a fatty substance called galactocerebroside. Without this enzyme, galactocerebroside accumulates in ...
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