Glycogen storage disease due to LAMP-2 deficiency (Q84779): Difference between revisions
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Doença de depósito de glicogênio devido a deficiência de LAMP-2 (Proteína 2 de Membrana Associada ao Lisossoma) é uma doença de depósito de glicogênio lisossomal caracterizada por miocardiopatia grave e vários graus de fraqueza muscular, frequentemente associada com comprometimento intelectual. | |||
| description / en | description / en | ||
Glycogen storage disease due to LAMP-2 (Lysosomal-Associated Membrane Protein 2) deficiency is a lysosomal glycogen storage disease characterised by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit. | |||
Revision as of 10:07, 15 August 2026
Glycogen storage disease due to LAMP-2 (Lysosomal-Associated Membrane Protein 2) deficiency is a lysosomal glycogen storage disease characterised by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_331119306 |
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| English | Glycogen storage disease due to LAMP-2 deficiency |
Glycogen storage disease due to LAMP-2 (Lysosomal-Associated Membrane Protein 2) deficiency is a lysosomal glycogen storage disease characterised by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit. |
