Galactosylceramide Lipidosis

It is feasible that the primary title of the record Leukodystrophy, Krabbe’s is not the name you anticipated.
Krabbe’s Leukodystrophy is an unusual acquired lipid storage space problem triggered by a shortage of the enzyme galactocerebrosidase (GALC), which is essential for the break down (metabolic rate) of the sphingolipids galactosylceremide as well as psychosine. This metabolic problem is identified by dynamic neurological disorder such as psychological retardation, paralysis, loss of sight, hearing problems and also paralysis of particular face muscle tissues (pseudobulbar palsy).

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