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Farber disease: a rare neurodegenerative disorder
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2009; 19 (1): 67-68
en Inglés | IMEMR | ID: emr-91588
ABSTRACT
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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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Encéfalo / Enfermedades Neurodegenerativas / Articulaciones / Mucolipidosis Tipo de estudio: Informe de Casos Límite: Humanos / Masculino Idioma: Inglés Revista: J. Coll. Physicians Surg. Pak. Año: 2009

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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Encéfalo / Enfermedades Neurodegenerativas / Articulaciones / Mucolipidosis Tipo de estudio: Informe de Casos Límite: Humanos / Masculino Idioma: Inglés Revista: J. Coll. Physicians Surg. Pak. Año: 2009