Literature DB >> 11483824

Case report: liver glycogen synthase deficiency--a cause of ketotic hypoglycemia.

S L Rutledge1, J Atchison, N U Bosshard, B Steinmann.   

Abstract

Glycogen synthase deficiency is a rare inborn error of metabolism, characterized by fasting hypoglycemia, hypoglycemic seizures, and ketonuria. Only 7 families with 14 affected children have been reported. Here, we report an additional patient with this deficiency. Findings in this patient were clinically and biochemically consistent with those reported in patients with ketotic hypoglycemia and may alert the clinician to consider glycogen synthase deficiency.

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Year:  2001        PMID: 11483824     DOI: 10.1542/peds.108.2.495

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  7 in total

1.  From hyperinsulinaemic hypoglycaemia to ketotic hypoglycaemia: the range of glucose abnormalities in patients born with intrauterine growth retardation.

Authors:  Inderpal Singh Kochar; Khalid Hussain
Journal:  Eur J Pediatr       Date:  2006-12-20       Impact factor: 3.183

Review 2.  Glycogen metabolism and glycogen storage disorders.

Authors:  Shibani Kanungo; Kimberly Wells; Taylor Tribett; Areeg El-Gharbawy
Journal:  Ann Transl Med       Date:  2018-12

3.  Ketotic hypoglycaemia in children with diazoxide responsive hyperinsulinism of infancy.

Authors:  Khalid Hussain
Journal:  Eur J Pediatr       Date:  2005-03-17       Impact factor: 3.183

Review 4.  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

5.  Novel GYS2 mutations in a Japanese patient with glycogen storage disease type 0a.

Authors:  Hiroyuki Iijima; Yasuhiko Ago; Ryoji Fujiki; Takaaki Takayanagi; Mitsuru Kubota
Journal:  Mol Genet Metab Rep       Date:  2021-01-10

6.  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

Review 7.  A patient with glycogen storage disease type 0 and a novel sequence variant in GYS2: a case report and literature review.

Authors:  Janez Jan Arko; Marusa Debeljak; Mojca Zerjav Tansek; Tadej Battelino; Urh Groselj
Journal:  J Int Med Res       Date:  2020-08       Impact factor: 1.671

  7 in total

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