PubMed · 2009 · 10 citations · 24 references
Neurodegenerative DiseasesNeurobiology Of DiseasePediatricsPathologyRare Neurodegenerative MucolipidosisDegenerative DiseaseNeurologyNeuropathologyMedicineFarber DiseaseCase Report
This is the case report of a two-and-a-half-year old male infant with Farber disease, which is a rare neurodegenerative mucolipidosis. The child presented with regression of milestones, laryngeal involvement and painful joints with swellings around the joints. Neuroimaging findings and the biopsy of the soft tissue swellings helped to reach the diagnosis.
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Subclass Restriction, Thymus-independent Type, Immunodeficiencies +20
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Farber disease: clinical presentation, pathogenesis and a new approach to treatment
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