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Farber disease (also known as Farber's lipogranulomatosis, acid ceramidase deficiency, "Lipogranulomatosis", [2] and ASAH1-related disorders) is an extremely rare, progressive, autosomal recessive lysosomal storage disease caused by a deficiency of the acid ceramidase enzyme.
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Enzyme replacement therapy is available to treat mainly Fabry disease and Gaucher disease, and people with these types of sphingolipidoses may live well into adulthood. The other types are generally fatal by age 1 to 5 years for infantile forms, but progression may be mild for juvenile- or adult-onset forms.
Mosby's Dictionary of Medicine, Nursing & Health Professions is a dictionary of health-related topics. The 8th edition, published in 2009, contains 2,240 pages and 2,400 colour illustrations. The 8th edition, published in 2009, contains 2,240 pages and 2,400 colour illustrations.
Cherry-red spot as seen here in Tay–Sachs disease, caused by the fovea's center appearing bright red because it is surrounded by a whiter than usual area. Metabolic Storage Diseases:, [6] [7] Tay–Sachs disease; Farber disease; GM1 and GM2 gangliosidoses; Metachromatic leukodystrophy; Niemann–Pick disease; Sandhoff disease; Sialidosis
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...
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