Episodic ataxia type 2 - CACNA1A mutation (Q90142): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Ataxia paroxística familiar é uma forma de ataxia cerebelar caracterizada por episódios agudos de ataxia, vertigem e náuseas, com duração variando de poucos minutos a muitas horas. Os episódios podem ser acompanhados por disartria, diplopia, distonia ou hemiplegia.
@@ description / en / description / en @@
+Familial paroxysmal ataxia is a form of cerebellar ataxia characterised by episodes of acute ataxia, dizziness and nausea, with a duration ranging from a few minutes to several hours. The episodes may be accompanied by dysarthria, diplopia, dystonia or hemiplegia.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1470995662
@@ Property / Canonical URI: https://id.who.int/icd/entity/1470995662 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1470995662
@@ Property / CURIE: CID11:ID_1470995662 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1470995662
@@ Property / Canary Token: dki-india-ID_1470995662 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 17:05, 15 August 2026

Familial paroxysmal ataxia is a form of cerebellar ataxia characterised by episodes of acute ataxia, dizziness and nausea, with a duration ranging from a few minutes to several hours. The episodes may be accompanied by dysarthria, diplopia, dystonia or hemiplegia.

Language	Label	Description	Also known as
default for all languages	ID_1470995662
English	Episodic ataxia type 2 - CACNA1A mutation	Familial paroxysmal ataxia is a form of cerebellar ataxia characterised by episodes of acute ataxia, dizziness and nausea, with a duration ranging from a few minutes to several hours. The episodes may be accompanied by dysarthria, diplopia, dystonia or hemiplegia.