Congenital myasthenia with presynaptic defect (Q92757): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1231819833 / rank | |||
Normal rank | |||
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. |
