What Causes The Krabbe Disease ?

Krabbe disease also referred as globoid cell leukodystrophy or galactosylceramide deficiency is a rare degenerative inherited disease that affects the central nervous system. People with Krabbe disease typically experiences increased muscle tone that causes muscle spasticity, awkwardness, poor motor skills, sight problem, seizures and poor auditory functions.More...

Krabbe Disease Symptoms

Krabbe disease is a rare genetic, hereditary disorder which affects the nervous system of the body. It can affect the muscle movement and also hearing loss. This disease is mostly found in children below the age of two; however older children may also get affected by it.  It affects only 1 out of 100,000 children and gets its name from the Danish neurologist who first reported the disease in 1916.More...

Krabbe Disease Treatment

A rare, genetic disorder of the central nervous system is known as Krabbe disease. This disease is inherited and over a period of time the brain of the person affected by this condition slowly dies due to lack of an enzyme called galactocerebrosidase (GALC).More...

History Of Krabbe Disease

Krabbe disease is a progressive, genetic disorder of the nervous system. This disease gets its name from Danish neurologist Knud Haraldsen Krabbe. He was the person who first described this disease in the period of 1913-1916. It is also known by the name of Globoid cell leukodystrophy. This condition may be found only in 1 out of 1,00,000 people.More...