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PedAM

Pediatric Disease Annotations & Medicines




Disease cystic fibrosis
Phenotype C0020456|hyperglycemia
Sentences 2
PubMedID- 21115768 Subjects who had at least one ogtt performed during the study period were identified as having normal glucose tolerance (ngt), igt, cystic fibrosis–related diabetes without fasting hyperglycemia (cfrd fh−) or cfrd with fasting hyperglycemia (cfrd fh+) by standard definitions (table 1).
PubMedID- 26003073 The patients were divided into groups based on glucose tolerance categories in the oral glucose tolerance test (impaired glucose tolerance - igt, cystic fibrosis related diabetes without fasting hyperglycemia - cfrd fh(-) or with fasting hyperglycemia - cfrd fh(+)).

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