Literature DB >> 20352251

Symptomatic paroxysmal dysarthria-ataxia in demyelinating diseases.

Christophe Marcel1, Mathieu Anheim, Constance Flamand-Rouvière, Françoise Heran, Pascal Masnou, Clotilde Boulay, Ivan Mari, Christine Tranchant, Emmanuel Roze.   

Abstract

Paroxysmal dysarthria-ataxia syndrome (PDA) is a rare neurological disorder that can be either primary or symptomatic of acute neurological dysfunction. Episodes of symptomatic PDA are poorly documented and there are no video reports. We describe the cases of two patients with symptomatic PDA related to demyelinating diseases. Detailed studies of the patients' speech disorders showed that the dysarthria and gait disorders were of the ataxic type in both cases. Both patients had midbrain lesions at or below the level of the red nucleus, confirming that this area is critically involved in PDA. The best clinical signs for distinguishing between symptomatic and primary PDA are adult onset and short (<1 min) episodes in the former. If these signs are present, brain MRI should be used to identify a cause of symptomatic PDA.

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Year:  2010        PMID: 20352251     DOI: 10.1007/s00415-010-5534-3

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  16 in total

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10.  Do oligoclonal bands add information to MRI in first attacks of multiple sclerosis?

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  6 in total

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5.  Isolated paroxysmal dysarthria caused by a single demyelinating midbrain lesion.

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Review 6.  Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.

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  6 in total

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