Paroxysmal nonkinesigenic dyskinesia
A hereditary autosomal dominant disorder characterized by episodes of involuntary movements involving the extremities, neck, trunk, or face. Onset is usually in infancy or childhood and episodes may be precipitated by alcohol, caffeine, fatigue, or stress. Mutations in the PNKD gene have been identified. OMIM: 118800
Also Known As:
Choreoathetosis familial paroxysmal; Choreoathetosis, Familial Paroxysmal; Choreoathetosis, Nonkinesigenic; Dystonia 8; Familial Paroxysmal Nonkinesigenic Dyskinesia; Familial paroxysmal choreoathetosis; Mount-Reback syndrome; Nonkinesigenic choreoathetosis; Paroxysmal Nonkinesigenic Dyskinesia 1; Paroxysmal dystonic choreoathetosis
Networked: 35
relevant articles (9 outcomes,
2 trials/studies)
Relationship Network
Disease Context: Research Results
Related Diseases
Experts
1. | Mink, Jonathan W:
2 articles
(06/2015 - 04/2010)
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2. | Fu, Ying-Hui:
2 articles
(03/2015 - 02/2012)
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3. | Shen, Yiguo:
2 articles
(03/2015 - 02/2012)
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4. | Rainier, Shirley:
2 articles
(04/2005 - 07/2004)
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5. | Abou Jamra, Rami:
1 article
(11/2020)
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6. | Gburek-Augustat, Janina:
1 article
(11/2020)
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7. | Heinze, Anja:
1 article
(11/2020)
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8. | Merkenschlager, Andreas:
1 article
(11/2020)
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9. | Bailey, Cole S:
1 article
(10/2019)
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10. | Keros, Sotirios:
1 article
(10/2019)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Paroxysmal nonkinesigenic dyskinesia:
Therapies and Procedures