farber lipogranulomatosis/silica

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Tissue accumulation of sulfatide and GM3 ganglioside in a patient with variant Farber disease.

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We analyzed the lipids in the tissues of a patient with an atypical form of Farber disease who developed several clinical symptoms not seen in patients with typical Farber disease (acid ceramidase deficiency). Lipids were extracted from formalin-fixed brain, liver and kidney and purified by ion

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