Literature DB >> 12072888

Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations.

Bert E Bachrach1, David A Weinstein, Marju Orho-Melander, Anne Burgess, Joseph I Wolfsdorf.   

Abstract

Although glycogen storage disease type 0 (GSD0) is included in the differential diagnosis of ketotic hypoglycemia, it usually is not considered in the evaluation of glucosuria or hyperglycemia. We describe two children with GSD0, confirmed by mutation analysis, who had glucosuria and hyperglycemia. Because of the variable presentation of this disorder and previous dependence on liver biopsy to confirm diagnosis, it is likely that GSD0 is underdiagnosed.

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Year:  2002        PMID: 12072888     DOI: 10.1067/mpd.2002.124317

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  13 in total

Review 1.  Approach to hypoglycemia in infants and children.

Authors:  Kajal Gandhi
Journal:  Transl Pediatr       Date:  2017-10

Review 2.  Hepatic glycogen synthase deficiency: an infrequently recognized cause of ketotic hypoglycemia.

Authors:  David A Weinstein; Catherine E Correia; Andrew C Saunders; Joseph I Wolfsdorf
Journal:  Mol Genet Metab       Date:  2005-12-06       Impact factor: 4.797

Review 3.  Biochemical and clinical aspects of glycogen storage diseases.

Authors:  Sara S Ellingwood; Alan Cheng
Journal:  J Endocrinol       Date:  2018-06-06       Impact factor: 4.286

4.  PTG gene deletion causes impaired glycogen synthesis and developmental insulin resistance.

Authors:  Sean M Crosson; Ahmir Khan; John Printen; Jeffrey E Pessin; Alan R Saltiel
Journal:  J Clin Invest       Date:  2003-05       Impact factor: 14.808

Review 5.  Glycogen storage diseases: new perspectives.

Authors:  Hasan Ozen
Journal:  World J Gastroenterol       Date:  2007-05-14       Impact factor: 5.742

6.  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

7.  A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0.

Authors:  Ana Priscila Soggia; Maria Lúcia Correa-Giannella; Maria Angela Henriques Fortes; Ana Mercedes Cavaleiro Luna; Maria Adelaide Albergaria Pereira
Journal:  BMC Med Genet       Date:  2010-01-05       Impact factor: 2.103

8.  PERSISTENT ASYMPTOMATIC SEVERE HYPOGLYCAEMIA DUE TO TYPE 0A GLYCOGENOSIS - GENERAL AND ORO-DENTAL ASPECTS.

Authors:  L Matei; M I Teodorescu; A Kozma; A D Iordan Dumitru; S M Stoicescu; S Carniciu
Journal:  Acta Endocrinol (Buchar)       Date:  2019 Oct-Dec       Impact factor: 0.877

9.  Pediatric patient with hyperketotic hypoglycemia diagnosed with glycogen synthase deficiency due to the novel homozygous mutation in GYS2.

Authors:  Edyta Szymańska; Dariusz Rokicki; Urszula Wątrobinska; Elżbieta Ciara; Paulina Halat; Rafał Płoski; Anna Tylki-Szymańka
Journal:  Mol Genet Metab Rep       Date:  2015-08-24

10.  Hepatic glycogen synthase (GYS2) deficiency: seven novel patients and seven novel variants.

Authors:  Elena A Kamenets; Elena A Gusarova; Natalia V Milovanova; Yulia S Itkis; Tatiana V Strokova; Maria A Melikyan; Irina V Garyaeva; Irina G Rybkina; Natalia V Nikitina; Ekaterina Y Zakharova
Journal:  JIMD Rep       Date:  2020-02-25
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