Congenital myasthenia with synaptic basal lamina defects (Q92751): Difference between revisions
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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. |
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CID11:ID_7881372
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dki-india-ID_7881372
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Concluído
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