Literature DB >> 23604616

Symptomatic west syndrome secondary to glucose transporter-1(GLUT1) deficiency with complete response to 4:1 ketogenic diet.

K N Vykuntaraju1, Srikanth Bhat, K S Sanjay, M Govindaraju.   

Abstract

Glucose transporter type 1 (GLUT-1) deficiency is a rare cause of preventable intellectual disability. Intellectual disability is due to refractory seizures in infancy and reduced supply of glucose to the brain. The authors report a third born male child of consanguineous parentage who presented with infantile spasms. Initially, he had refractory convulsions of focal, generalised, and myoclonic jerks, not responding to multiple anticonvulsants. He also had choreoathetoid movements. On examination he had microcephaly. MRI of brain was normal and EEG showing diffuse slowing. CSF glucose was low compared to blood glucose, with normal lactate and without any cells, hence diagnosed as Glucose transporter-1 deficiency and started on ketogenic diet. With ketogenic diet, child was seizure free, anticonvulsants decreased to 2 from 5, and improvements in development were noted.

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Year:  2013        PMID: 23604616     DOI: 10.1007/s12098-013-1044-5

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  6 in total

1.  Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay.

Authors:  D C De Vivo; R R Trifiletti; R I Jacobson; G M Ronen; R A Behmand; S I Harik
Journal:  N Engl J Med       Date:  1991-09-05       Impact factor: 91.245

2.  GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier.

Authors:  G Seidner; M G Alvarez; J I Yeh; K R O'Driscoll; J Klepper; T S Stump; D Wang; N B Spinner; M J Birnbaum; D C De Vivo
Journal:  Nat Genet       Date:  1998-02       Impact factor: 38.330

3.  Glucose transporter type I deficiency syndrome: epilepsy phenotypes and outcomes.

Authors:  Amanda W Pong; Brianna R Geary; Kris M Engelstad; Ashwini Natarajan; Hong Yang; Darryl C De Vivo
Journal:  Epilepsia       Date:  2012-07-19       Impact factor: 5.864

4.  Atypical GLUT1 deficiency with prominent movement disorder responsive to ketogenic diet.

Authors:  Jennifer R L Friedman; Elizabeth A Thiele; Dong Wang; Kara B Levine; Erin K Cloherty; Heidi H Pfeifer; Darryl C De Vivo; Anthony Carruthers; Marvin R Natowicz
Journal:  Mov Disord       Date:  2006-02       Impact factor: 10.338

5.  Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.

Authors:  Dong Wang; Juan M Pascual; Hong Yang; Kristin Engelstad; Sarah Jhung; Ruo Peng Sun; Darryl C De Vivo
Journal:  Ann Neurol       Date:  2005-01       Impact factor: 10.422

6.  Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

Authors:  Arvid Suls; Peter Dedeken; Karolien Goffin; Hilde Van Esch; Patrick Dupont; David Cassiman; Judith Kempfle; Thomas V Wuttke; Yvonne Weber; Holger Lerche; Zaid Afawi; Wim Vandenberghe; Amos D Korczyn; Samuel F Berkovic; Dana Ekstein; Sara Kivity; Philippe Ryvlin; Lieve R F Claes; Liesbet Deprez; Snezana Maljevic; Alberto Vargas; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Koen Van Laere; Peter De Jonghe; Wim Van Paesschen
Journal:  Brain       Date:  2008-06-24       Impact factor: 13.501

  6 in total
  3 in total

Review 1.  Infantile spasm: a review article.

Authors:  Mohammad Mahdi Taghdiri; Hamid Nemati
Journal:  Iran J Child Neurol       Date:  2014

2.  Glucose transport 1 deficiency presenting as infantile spasms with a mutation identified in exon 9 of SLC2A1.

Authors:  Hyun Hee Lee; Yun Jung Hur
Journal:  Korean J Pediatr       Date:  2016-11-30

Review 3.  Metabolic etiologies in West syndrome.

Authors:  Seda Salar; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2018-03-14
  3 in total

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