Glycogen storage disease due to glucose-6-phosphatase deficiency (Q100832): Difference between revisions
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A glicogenose causada por deficiência da glicose-6-fosfatase (G6P) tipo b, ou doença de armazenamento do glicogênio tipo 1b, é um tipo de glicogenose devido a deficiência de G6P associando características da glicogenose tipo a com neutropenia e disfunção neutrofílica, que aumentam a tendência a infecções, gengivoestomatite aftosa recorrente e doença inflamatória intestinal. | |||
| description / en | description / en | ||
Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency associating the clinical features of glycogenosis due to G6P deficiency type a to neutropaenia, and neutrophil dysfunction that are responsible for tendency towards infections, relapsing aphthous gingivostomatitis, and inflammatory bowel disease. | |||
Revision as of 17:36, 16 August 2026
Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency associating the clinical features of glycogenosis due to G6P deficiency type a to neutropaenia, and neutrophil dysfunction that are responsible for tendency towards infections, relapsing aphthous gingivostomatitis, and inflammatory bowel disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_377675277 |
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| English | Glycogen storage disease due to glucose-6-phosphatase deficiency |
Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency associating the clinical features of glycogenosis due to G6P deficiency type a to neutropaenia, and neutrophil dysfunction that are responsible for tendency towards infections, relapsing aphthous gingivostomatitis, and inflammatory bowel disease. |
