About The Medical Condition Galactosylceramidase Deficiency Diseases

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Find the definition of the medical term Galactosylceramidase Deficiency Diseases. Galactosylceramidase Deficiency Diseases defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.

Galactosylceramidase Deficiency Diseases

Galactosylceramidase Deficiency Diseases Medical Condition Defined & Explained
Galactosylceramidase Deficiency Diseases Medical Condition

What's The Definition Of The Medical Condition Galactosylceramidase Deficiency Diseases?

An autosomal recessive inherited sphingolipidosis caused by a deficiency of GALACTOSYLCERAMIDASE leading to an accumulation of PSYCHOSINE in LYSOSOMES of the BRAIN; PERIPHERAL NERVES; LIVER; KIDNEY; and LEUKOCYTES. In the nervous sytem there is prominent central and peripheral demyelination. The infantile form presents at age 4-6 months with psychomotor retardation, MUSCLE SPASTICITY, and tonic spasms induced by minor stimuli. Death occurs within two years. Later onset forms of this disease are characterized by a less fulminant course. (From Menkes, Textbook of Child Neurology, 5th ed, pp195-7)

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