Galactocerebrosidase (GALC) Deficiency

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

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