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Identification of GCK-MODY in cases of neonatal hyperglycemia: a case series and review of clinical features
Heterozygous mutations in GCK result in a persistent, mildly raised glucose from birth, but it is usually diagnosed in adulthood as maturity-onset diabetes of the young (MODY), where hyperglycemia is often an incidental finding. The hyperglycemia of GCK-MODY is benign and does not require treatment,...
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| Veröffentlicht in: | Pediatr Diabetes |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7611537/ https://ncbi.nlm.nih.gov/pubmed/34085361 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pedi.13239 |
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