Prolonged episodes of hypoglycaemia in HNF4A-MODY mutation carriers with IGT. Evidence of persistent hyperinsulinism into early adulthood-Reference-Cited by-同舟云学术

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Prolonged episodes of hypoglycaemia in HNF4A-MODY mutation carriers with IGT. Evidence of persistent hyperinsulinism into early adulthood

Published:2016-08-23 Issue:6 Volume:53 Page:965-972
ISSN:0940-5429
Container-title:Acta Diabetologica
language:en
Short-container-title:Acta Diabetol

Author:

Bacon S.,Kyithar M. P.,Condron E. M.,Vizzard N.,Burke M.,Byrne M. M.

Funder

Health Research Board

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00592-016-0890-9.pdf

Reference40 articles.

1. Frayling TM, Evans JC, Bulman MP et al (2001) Beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors. Diabetes 50(Suppl 1):S94–S100

2. Antosik K, Gnys P, De Franco E et al (2016) Single patient in GCK-MODY family successfully re-diagnosed into GCK-PNDM through targeted next-generation sequencing technology. Acta Diabetol 53:337–338

3. Alkorta-Aranburu G, Carmody D, Cheng YW et al (2014) Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach. Mol Genet Metab 113:315–320

4. Ellard S, Lango Allen H, De Franco E et al (2013) Improved genetic testing for monogenic diabetes using targeted next-generation sequencing. Diabetologia 56:1958–1963

5. Kyithar MP, Bacon S, Pannu KK et al (2011) Identification of HNF1A-MODY and HNF4A-MODY in Irish families: phenotypic characteristics and therapeutic implications. Diabetes Metab 37:512–519

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1. Management of pregnancy in women with monogenic diabetes due to mutations in GCK, HNF1A and HNF4A genes;Frontiers in Genetics;2024-06-12

2. Variable phenotypes of individual and family monogenic cases with hyperinsulinism and diabetes: a systematic review;Reviews in Endocrine and Metabolic Disorders;2022-08-23

3. How do I diagnose Maturity Onset Diabetes of the Young in my patients?;Clinical Endocrinology;2022-05-02

4. Clinical and genetic heterogeneity of HNF4A/HNF1A mutations in a multicentre paediatric cohort with hyperinsulinaemic hypoglycaemia;European Journal of Endocrinology;2022-04-01

5. A novel HNF4A mutation identified in a child with maturity onset diabetes of the young;World Journal of Pediatrics;2022-02-03

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