Congenital myasthenia with presynaptic defect (Q92757): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1231819833
@@ Property / Canonical URI: https://id.who.int/icd/entity/1231819833 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1231819833
@@ Property / CURIE: CID11:ID_1231819833 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1231819833
@@ Property / Canary Token: dki-india-ID_1231819833 / 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 +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 07:53, 16 August 2026

The purely presynaptic CMS are least frequent, accounting for only 6% of all cases, include defects in evoked release of acetylcholine (ACh) quanta or ACh resynthesis due to choline acetyltransferase, paucity of synaptic vesicles and Lambert-Eaton-like CMS.

Language	Label	Description	Also known as
default for all languages	ID_1231819833
English	Congenital myasthenia with presynaptic defect	The purely presynaptic CMS are least frequent, accounting for only 6% of all cases, include defects in evoked release of acetylcholine (ACh) quanta or ACh resynthesis due to choline acetyltransferase, paucity of synaptic vesicles and Lambert-Eaton-like CMS.