Leukodystrophy, Globoid Cell, Late-Onset Medical Condition Defined & Explained

About The Medical Condition Leukodystrophy, Globoid Cell, Late-Onset

Find the definition of the medical term Leukodystrophy, Globoid Cell, Late-Onset. Leukodystrophy, Globoid Cell, Late-Onset defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.

Leukodystrophy, Globoid Cell, Late-Onset

Leukodystrophy, Globoid Cell, Late-Onset Medical Condition
What's The Definition Of The Medical Condition Leukodystrophy, Globoid Cell, Late-Onset? 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)

Leukodystrophy, Globoid Cell, Late-Onset Medical Condition

What's The Definition Of The Medical Condition Leukodystrophy, Globoid Cell, Late-Onset?

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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