Congenital myasthenia with synaptic basal lamina defects (Q92751): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A síndrome miastênica congênita associada à lâmina basal sináptica é responsável por 1 a 15% dos casos de miastenia e inclui deficiência de acetilecolinesterase da placa motora, deficiência de laminina α2 e anomalia da agrina. | |||
| description / en | description / en | ||
Synaptic basal lamina-associated congenital myasthenic syndrome accounts for 1—15% of myasthenic cases and includes endplate acetylecholinesterase deficiency, Laminin α2 deficiency and Agrin anomaly. | |||
Revision as of 07:52, 16 August 2026
Synaptic basal lamina-associated congenital myasthenic syndrome accounts for 1—15% of myasthenic cases and includes endplate acetylecholinesterase deficiency, Laminin α2 deficiency and Agrin anomaly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_7881372 |
||
| English | Congenital myasthenia with synaptic basal lamina defects |
Synaptic basal lamina-associated congenital myasthenic syndrome accounts for 1—15% of myasthenic cases and includes endplate acetylecholinesterase deficiency, Laminin α2 deficiency and Agrin anomaly. |
