Epilepsy of infancy with migrating focal seizures (Q41207): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1727727812
@@ Property / Canonical URI: https://id.who.int/icd/entity/1727727812 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8A61.12
@@ Property / CURIE: CID11:8A61.12 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8A61.12
@@ Property / Canary Token: dki-india-8A61.12 / 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

Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be found. The EEG shows multifocal, varying sites of seizure onset, and diffuse slowing.

Language	Label	Description	Also known as
default for all languages	8A61.12
English	Epilepsy of infancy with migrating focal seizures	Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be found. The EEG shows multifocal, varying sites of seizure onset, and diffuse slowing.