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A Case of Fly Catcher's Tongue Phenomenon in Hallervorden-Spatz Disease
Article en Ko | WPRIM | ID: wpr-12680
Biblioteca responsable: WPRO
ABSTRACT
Hallervorden-Spatz disease (HSD) is a rare, progressive, autosomal recessive hereditary disorder characterized by pyramidal and extrapyramidal signs, speech disturbances, mental deterioration and retinal degeneration during childhood or adolescence. In late-onset form after the age of 20, parkinsonian features may be the predominant clinical manifestation. Meanwhile, involuntary tongue movements are rare and poorly understood, which have been reported in tardive dyskinesia, neuroacanthocytosis, chronic epilepsy, and after head trauma. We report a case of a patient with 'fly catcher's tongue' as a major clinical presentation, accompanied with mild parkinsonism, and typical MR findings of HSD.
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Texto completo: 1 Índice: WPRIM Asunto principal: Degeneración Retiniana / Lengua / Trastornos Parkinsonianos / Dípteros / Epilepsia / Neuroacantocitosis / Neurodegeneración Asociada a Pantotenato Quinasa / Traumatismos Craneocerebrales / Trastornos del Movimiento Límite: Adolescent / Humans Idioma: Ko Revista: Journal of the Korean Neurological Association Año: 2000 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Degeneración Retiniana / Lengua / Trastornos Parkinsonianos / Dípteros / Epilepsia / Neuroacantocitosis / Neurodegeneración Asociada a Pantotenato Quinasa / Traumatismos Craneocerebrales / Trastornos del Movimiento Límite: Adolescent / Humans Idioma: Ko Revista: Journal of the Korean Neurological Association Año: 2000 Tipo del documento: Article