Glycogen storage disease due to acid maltase deficiency, adult onset (Q100840): Difference between revisions
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Doença de depósito de glicogênio devido à deficiência de maltase ácida, de início tardio, é uma miopatia metabólica degenerativa que afeta particularmente os músculos respiratórios e esqueléticos . É caracterizada por acúmulo de glicogênio nos lisossomos. | |||
| description / en | description / en | ||
Glycogen storage disease due to acid maltase deficiency, late onset, a form of Glycogen storage disease due to acid maltase deficiency, a degenerative metabolic myopathy particularly affecting respiratory and skeletal muscles, is characterised by an accumulation of glycogen in lysosomes. | |||
Revision as of 17:36, 16 August 2026
Glycogen storage disease due to acid maltase deficiency, late onset, a form of Glycogen storage disease due to acid maltase deficiency, a degenerative metabolic myopathy particularly affecting respiratory and skeletal muscles, is characterised by an accumulation of glycogen in lysosomes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1258887500 |
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| English | Glycogen storage disease due to acid maltase deficiency, adult onset |
Glycogen storage disease due to acid maltase deficiency, late onset, a form of Glycogen storage disease due to acid maltase deficiency, a degenerative metabolic myopathy particularly affecting respiratory and skeletal muscles, is characterised by an accumulation of glycogen in lysosomes. |
