Literature DB >> 8308231

Ketotic hypoglycemia: a case report.

E S Pollack1, C V Pollack.   

Abstract

Ketotic hypoglycemia (KH) is recognized in the pediatric literature as the most common cause of childhood hypoglycemia. Since the first manifestation of the syndrome is classically that of new onset seizures, initial emergency department presentation is likely. We describe a representative case and emphasize the importance of routine serum glucose and urine ketone measurements in young children with new onset seizures.

Entities:  

Mesh:

Year:  1993        PMID: 8308231     DOI: 10.1016/0736-4679(93)90306-r

Source DB:  PubMed          Journal:  J Emerg Med        ISSN: 0736-4679            Impact factor:   1.484


  2 in total

1.  Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in children.

Authors:  Laurie M Brown; Michelle M Corrado; Rixt M van der Ende; Terry G J Derks; Margaret A Chen; Sara Siegel; Kate Hoyt; Catherine E Correia; Christopher Lumpkin; Theresa B Flanagan; Caroline T Carreras; David A Weinstein
Journal:  J Inherit Metab Dis       Date:  2014-07-29       Impact factor: 4.982

2.  Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in children.

Authors:  Yazeid Alhaidan; Martin J Larsen; Anders Jørgen Schou; Maria H Stenlid; Mohammed A Al Balwi; Henrik Thybo Christesen; Klaus Brusgaard
Journal:  Sci Rep       Date:  2020-02-07       Impact factor: 4.379

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.