Dravet syndrome (Q41208): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Encefalopatia epiléptica refratária que ocorre em bebês saudáveis durante o primeiro ano de vida com crises epilépticas clônicas, tônico-clônicas generalizadas e crises epilépticas unilaterais, hemiclônicas ou estado de mal epiléptico generalizado. O EEG interictal pode ser inicialmente normal, porém com o tempo a atividade de base se deteriora e aparecem paroxismos de polipontas bilaterais assimétricos focais ou multifocais, e ondas lentas. Mutações do gene do canal de sódio voltagem-dependente SCNA1 são comumente encontradas.
@@ description / en / description / en @@
+A refractory epileptic encephalopathy occurring in otherwise healthy infants during the first year of life with clonic/tonic-clonic, generalised and unilateral seizures, hemiclonic or generalised status epilepticus. The interictal EEG may initially be normal but with time background activity deteriorates and bilateral asymmetric, focal or multifocal paroxysms of polyspike and slow-waves appear. Mutations in the voltage-gated sodium channel gene SCN1A are commonly found.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1255654700
@@ Property / Canonical URI: https://id.who.int/icd/entity/1255654700 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8A61.11
@@ Property / CURIE: CID11:8A61.11 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8A61.11
@@ Property / Canary Token: dki-india-8A61.11 / 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
@@ Property / Linked ICD 10 @@
+G40.0
@@ Property / Linked ICD 10: G40.0 / rank @@
+Normal rank

Latest revision as of 07:16, 13 August 2026

A refractory epileptic encephalopathy occurring in otherwise healthy infants during the first year of life with clonic/tonic-clonic, generalised and unilateral seizures, hemiclonic or generalised status epilepticus. The interictal EEG may initially be normal but with time background activity deteriorates and bilateral asymmetric, focal or multifocal paroxysms of polyspike and slow-waves appear. Mutations in the voltage-gated sodium channel gene SCN1A are commonly found.

Language	Label	Description	Also known as
default for all languages	8A61.11
English	Dravet syndrome	A refractory epileptic encephalopathy occurring in otherwise healthy infants during the first year of life with clonic/tonic-clonic, generalised and unilateral seizures, hemiclonic or generalised status epilepticus. The interictal EEG may initially be normal but with time background activity deteriorates and bilateral asymmetric, focal or multifocal paroxysms of polyspike and slow-waves appear. Mutations in the voltage-gated sodium channel gene SCN1A are commonly found.