Paroxysmal dyskinesia

Paroxysmal dyskinesia

The paroxysmal dyskinesias are a group of rare movement disorders characterized by attacks of hyperkinesis with intact consciousness. [ Blueprints Neurolgy, 2nd ed.]

Types

* Paroxysmal kinesogenic choreoathetosis
* Paroxysmal nonkinesogenic dyskinesia
* Paroxysmal exercise-induced dystonia

References


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  • Paroxysmal kinesogenic choreoathetosis — (PKC) is a type of paroxysmal dyskinesia characterized by episodes of chorea, athetosis, or dystonia, triggered by sudden movements. Episodes last for seconds to minutes. The paroxysmal dyskinesias are a group of rare movement disorders… …   Wikipedia

  • Paroxysmal exercise-induced dystonia — is a type of paroxysmal dyskinesia characterized by episodes of dystonia induced by sustained exercise. Episodes may last for several hours. The paroxysmal dyskinesias are a group of rare movement disorders characterized by attacks of… …   Wikipedia

  • Paroxysmal nonkinesigenic dyskinesia — Classification and external resources OMIM 118800 DiseasesDB 32382 Paroxysmal Nonkinesigenic Dyskinesia (PNKD) is an episodic move …   Wikipedia

  • Paroxysmal Nonkinesigenic Dyskinesia — (PNKD) is an episodic movement disorder first described by Mount and Reback in 1940 under the name Familial paroxysmal choreoathetosis [Mount, L. A.; Reback, S. : Familial paroxysmal choreoathetosis: preliminary report on a hitherto undescribed… …   Wikipedia

  • paroxysmal kinesigenic dyskinesia — brief episodes of dyskinesia caused by sudden movements, hyperventilation, or a sudden stimulus …   Medical dictionary

  • PNKD — Paroxysmal nonkinesiogenic dyskinesia, also known as PNKD, is a human gene.cite web | title = Entrez Gene: PNKD paroxysmal nonkinesiogenic dyskinesia| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=25953|… …   Wikipedia

  • SLC16A2 — Solute carrier family 16, member 2 (monocarboxylic acid transporter 8), also known as SLC16A2, is a human gene.cite web | title = Entrez Gene: SLC16A2 solute carrier family 16, member 2 (monocarboxylic acid transporter 8)| url =… …   Wikipedia

  • FGF14 — Fibroblast growth factor 14, also known as FGF14, is a human gene.cite web | title = Entrez Gene: FGF14 fibroblast growth factor 14| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2259| accessdate = ] PBB… …   Wikipedia

  • Dystonia — Dystonias Classification and external resources A person with medication induced dystonia. ICD 10 G24.9 …   Wikipedia

  • List of diseases (P) — A list of diseases in the English Wikipedia.DiseasesTOC PaPac Pal* Pachydermoperiostosis * Pachygyria * Pachyonychia congenita Jackson Lawler type * Pacman dysplasia * Paes Whelan Modi syndrome * Paget disease extramammary * Paget disease… …   Wikipedia

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