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8p22-p21.3 Google OMIM Orphanet PubMed Who named it? Wikipedia Farber lipogranulomatosis *Gene map locus 8p22-p21.3 Acid ceramidase deficiency Ceramidase deficiency Farber disease N-laurylsphingosine deacylase deficiency [Clinical features: subcutaneous nodules; arthritis; laryngeal involvement; mental retardation; macular degeneration] [Inheritance: autosomal recessive] |
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Disseminated Lipogranulomatosis |
Disseminated Lipogranulomatosis |
Disseminated Lipogranulomatosis |
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Indian Pediatrics |
Indian Pediatrics |
Indian Pediatrics |
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Farber’s disease |
Farber’s disease |
Farber Disease - Hepatosplenomegaly |
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Indian Pediatrics |
Indian Pediatrics |
LysoSomal Learning |
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Farber Disease - Lymphadenopathy |
Farber Disease - Swollen joints |
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LysoSomal Learning |
LysoSomal Learning |