Essential myoclonus (Q41094): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Forma hereditária de mioclonia, que não está usualmente associada a epilepsia ou a qualquer outra condição clínica. Mioclonia essencial tende a ser estável sem piorar de gravidade ao longo do tempo. Mais recentemente, acredita-se que a mioclonia essencial pode ser o mesmo que a distonia-mioclônica causada por uma mutação no gene sarcoglicano.
@@ description / en / description / en @@
+This is a hereditary form of myoclonus, which is not usually associated with epilepsy or any other medical condition. Essential myoclonus tends to be stable without increasing in severity over time. More recently, it is believed that essential myoclonus may be the same as myoclonus-dystonia caused by a mutation in the sarcoglycan gene.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/179893645
@@ Property / Canonical URI: https://id.who.int/icd/entity/179893645 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8A06.0
@@ Property / CURIE: CID11:8A06.0 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8A06.0
@@ Property / Canary Token: dki-india-8A06.0 / 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 @@
+G25.3
@@ Property / Linked ICD 10: G25.3 / rank @@
+Normal rank

Latest revision as of 07:09, 13 August 2026

This is a hereditary form of myoclonus, which is not usually associated with epilepsy or any other medical condition. Essential myoclonus tends to be stable without increasing in severity over time. More recently, it is believed that essential myoclonus may be the same as myoclonus-dystonia caused by a mutation in the sarcoglycan gene.

Language	Label	Description	Also known as
default for all languages	8A06.0
English	Essential myoclonus	This is a hereditary form of myoclonus, which is not usually associated with epilepsy or any other medical condition. Essential myoclonus tends to be stable without increasing in severity over time. More recently, it is believed that essential myoclonus may be the same as myoclonus-dystonia caused by a mutation in the sarcoglycan gene.