What is the role of enzyme ceramidase in the treatment of Farber disease?

A Breaking down ceramides
B Synthesizing sphingolipids
C Regulating lipid metabolism
D Inhibiting apoptosis
Farber disease is a rare genetic disorder caused by a deficiency of the enzyme ceramidase, which breaks down ceramides. Treatment involves replacing this enzyme to reduce ceramide accumulation.
OMIM Database
Enzymes in Disease Biochemistry Lysosomal Storage Diseases Hard MEDICAL Confidence: high