A rare inherited biochemical disorder involving the deficiency of an enzyme called ceramidase resulting in the harmful accumulation of certain chemicals in the body which causes damage and inflammation.
Farber's disease includes the 14 symptoms listed below:*psychomotor deterioration*subcutaneous nodules*failure to thrive*swollen joints*mental retardation*enlarged liver and spleen*hoarseness*painful joint swelling*joint deformity*breathing difficulty*cherry-red macular spots*eye granulomas*impaired deep tendon reflexes*impaired psychomotor development
- Genetic conditions
- Metabolic conditions
- Congenital conditions - metabolic disorders
- Congenital conditions
- Lipid metabolism conditions