Vol 71, No 4 (2020)
Clinical vignette
Published online: 2020-05-22

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Neonatal diabetes — same disease, same gene, different outcomes

Vicente Rey y Formoso1, Daniela Salazar2, Sofia Ferreira3, Rita Santos Silva3, Carla Costa3, Cíntia Castro Correia3
Pubmed: 32598018
Endokrynol Pol 2020;71(4):363-364.

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References

  1. Ashcroft FM, Puljung MC, Vedovato N. Neonatal Diabetes and the K Channel: From Mutation to Therapy. Trends Endocrinol Metab. 2017; 28(5): 377–387.
  2. Barbetti F, D'Annunzio G. Genetic causes and treatment of neonatal diabetes and early childhood diabetes. Best Pract Res Clin Endocrinol Metab. 2018; 32(4): 575–591.
  3. De Franco E, Ellard S. Genome, Exome, and Targeted Next-Generation Sequencing in Neonatal Diabetes. Pediatr Clin North Am. 2015; 62(4): 1037–1053.
  4. Lemelman MB, Letourneau L, Greeley SA. Neonatal Diabetes Mellitus: An Update on Diagnosis and Management. Clin Perinatol. 2018; 45(1): 41–59.
  5. Letourneau LR, Greeley SA. Precision Medicine: Long-Term Treatment with Sulfonylureas in Patients with Neonatal Diabetes Due to KCNJ11 Mutations. Curr Diab Rep. 2019; 19(8): 52.