Paroxysmal dyskinesia
Synonyms: Paroxysmal choreoathetosis · Paroxysmal dystonic choreoathetosis
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Autosomal dominant, Not applicable
- Age of onset
- Childhood
- Status
- active
Paroxysmal dyskinesia (PD) is a rare heterogenous group of movement disorders manifesting as abnormal involuntary movements that recur episodically and last only a brief time. PD includes paroxysmal kinesigenic dyskinesia (PKD), paroxysmal non-kinesigenic dyskinesia (PNKD), paroxysmal exertion-induced dyskinesia (PED) and a variant form of PKD, infantile convulsion and choreoathetosis (ICCA syndrome).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Paroxysmal dyskinesia | Paroxysmal choreoathetosis · Paroxysmal dystonic choreoathetosis |
| fr | Dyskinésie paroxystique | Choréoathétose paroxystique · Choréoathétose paroxystique dystonique |
| de | Dyskinesie, paroxysmale | Paroxysmale Choreoathetose · Paroxysmale dystone Choreoathetose |
| es | Discinesia paroxística | Coreoatetosis paroxística · Coreoatetosis paroxística distónica |
| it | Discinesia parossistica | Coreoatetosi distonica parossistica · Coreoatetosi parossistica |
| nl | Paroxysmale dyskinesie | Paroxysmale choreoathetose · Paroxysmale dystonische choreoathetose |
| pt | Discinesia paroxística | |
| pl | Dyskineza napadowa | Choreoatetoza napadowa · Napadowa choreoatetoza dystoniczna |
| cs | Paroxysmální dyskineze | Paroxysmální choreoatetóza · Paroxysmální dystonická choreoatetóza |
| uk | Пароксизмальна дискінезія | Пароксизмальний хореоатетоз · Пароксизмальний дистонічний хореоатетоз |
| zh | 阵发性运动障碍 | 阵发性张力障碍性舞蹈手足徐动症 |
| tr | Paroksismal diskinezi | Paroksismal koreoatetoz · Paroksismal distonik koreoatetoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015427 | E | validated | |
| MONDO | 15427 | E | validated | |
| MeSH | D002819 | E | validated | |
| UMLS | C0752210 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:200037Paroxysmal dystonia
rare genetic diseases; rare neurological diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1431
- This record as JSON: /data/d/1431.json