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Rare paroxysmal movement disorder

MedGen UID:
1843170
•Concept ID:
C5681054
•
Disease or Syndrome
Orphanet: ORPHA306768

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVRare paroxysmal movement disorder

Professional guidelines

PubMed

CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.
Indelicato E, Boesch S
Handb Exp Pharmacol 2023;279:227-248. doi: 10.1007/164_2022_625. PMID: 36592223
Episodic movement disorders: from phenotype to genotype and back.
Brockmann K
Curr Neurol Neurosci Rep 2013 Oct;13(10):379. doi: 10.1007/s11910-013-0379-7. PMID: 23963607
Treatment of paroxysmal dyskinesias.
Strzelczyk A, Bürk K, Oertel WH
Expert Opin Pharmacother 2011 Jan;12(1):63-72. Epub 2010 Nov 26 doi: 10.1517/14656566.2010.513971. PMID: 21108579

Recent clinical studies

Etiology

A rare paroxysmal movement disorder: mixed type of paroxysmal dyskinesia.
Sen A, Atakli D, Guresci B, Arpaci B
Ideggyogy Sz 2014 Nov 30;67(11-12):426-9. PMID: 25720246

Diagnosis

A rare paroxysmal movement disorder: mixed type of paroxysmal dyskinesia.
Sen A, Atakli D, Guresci B, Arpaci B
Ideggyogy Sz 2014 Nov 30;67(11-12):426-9. PMID: 25720246
Paroxysmal dystonia and paroxysmal tremor in a young patient with multiple sclerosis.
Nardocci N, Zorzi G, Savoldelli M, Rumi V, Angelini L
Ital J Neurol Sci 1995 Jun;16(5):315-9. doi: 10.1007/BF02249107. PMID: 8537220

Therapy

A rare paroxysmal movement disorder: mixed type of paroxysmal dyskinesia.
Sen A, Atakli D, Guresci B, Arpaci B
Ideggyogy Sz 2014 Nov 30;67(11-12):426-9. PMID: 25720246
Paroxysmal dystonia and paroxysmal tremor in a young patient with multiple sclerosis.
Nardocci N, Zorzi G, Savoldelli M, Rumi V, Angelini L
Ital J Neurol Sci 1995 Jun;16(5):315-9. doi: 10.1007/BF02249107. PMID: 8537220

Prognosis

A rare paroxysmal movement disorder: mixed type of paroxysmal dyskinesia.
Sen A, Atakli D, Guresci B, Arpaci B
Ideggyogy Sz 2014 Nov 30;67(11-12):426-9. PMID: 25720246

Clinical prediction guides

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.
Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB
Brain 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. PMID: 11004121

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

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    Consumer resources

    Reviews

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