Glycogen storage disease due to acid maltase deficiency, juvenile onset (Q100841): Difference between revisions
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Doença de depósito de glicogênio devido a deficiência de maltase ácida forma infantil não clássica (início na juventude) é uma doença de depósito de glicogênio devido à deficiência de maltase ácida. Trata-se de miopatia metabólica que afeta os músculos respiratórios e esqueléticos o que pode levar a comprometimento fatal da função respiratória durante a infância ou juventude. | |||
| description / en | description / en | ||
Glycogen storage disease due to acid maltase deficiency, non-classical infantile onset, is form of glycogen storage disease due to acid maltase deficiency, a metabolic myopathy affecting respiratory and skeletal muscles that may fatally impede respiratory function during childhood. | |||
Revision as of 17:37, 16 August 2026
Glycogen storage disease due to acid maltase deficiency, non-classical infantile onset, is form of glycogen storage disease due to acid maltase deficiency, a metabolic myopathy affecting respiratory and skeletal muscles that may fatally impede respiratory function during childhood.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1193859896 |
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| English | Glycogen storage disease due to acid maltase deficiency, juvenile onset |
Glycogen storage disease due to acid maltase deficiency, non-classical infantile onset, is form of glycogen storage disease due to acid maltase deficiency, a metabolic myopathy affecting respiratory and skeletal muscles that may fatally impede respiratory function during childhood. |
