"' Farber disease "'( also known as "'Farber's lipogranulomatosis "', "'ceramidase deficiency "', " Fibrocytic dysmucopolysaccharidosis, " and " Lipogranulomatosis " ) is an extremely rare ( 80 cases reported worldwide to this day ) autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase that causes an accumulation of fatty material sphingolipids leading to abnormalities in the joints, liver, throat, tissues and central nervous system.
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"' Farber disease "'( also known as "'Farber's lipogranulomatosis "', "'ceramidase deficiency "', " Fibrocytic dysmucopolysaccharidosis, " and " Lipogranulomatosis " ) is an extremely rare ( 80 cases reported worldwide to this day ) autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase that causes an accumulation of fatty material sphingolipids leading to abnormalities in the joints, liver, throat, tissues and central nervous system.
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