Literature DB >> 14605501

GLUT-1 deficiency without epilepsy--an exceptional case.

W C G Overweg-Plandsoen1, J E M Groener, D Wang, W Onkenhout, O F Brouwer, H D Bakker, D C De Vivo.   

Abstract

The GLUT-1 deficiency is a metabolic disorder caused by a defect in glucose transport across the blood-brain barrier as a result of a defect in the glucose-transport protein. Patients present with epileptic seizures, delayed development, ataxia and hypotonia, and in many cases acquired microcephaly. In most patients, treatment with a ketogenic diet proved to be successful in controlling the epilepsy. We report a 9-year-old boy with retardation and ataxia, but without epilepsy, caused by GLUT-1 deficiency, proven biochemically and by DNA analysis. Treatment with a medium-chain triglyceride ketogenic diet had a beneficial effect.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14605501     DOI: 10.1023/a:1025999914822

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  10 in total

1.  Glucose transporter type 1 deficiency: a study of two cases with video-EEG.

Authors:  R G Boles; M R Seashore; W G Mitchell; P R Kollros; S Mofidi; E J Novotny
Journal:  Eur J Pediatr       Date:  1999-12       Impact factor: 3.183

2.  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

3.  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

4.  Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35.

Authors:  T B Shows; R L Eddy; M G Byers; Y Fukushima; C R Dehaven; J C Murray; G I Bell
Journal:  Diabetes       Date:  1987-04       Impact factor: 9.461

5.  Autosomal dominant transmission of GLUT1 deficiency.

Authors:  J Klepper; M Willemsen; A Verrips; E Guertsen; R Herrmann; C Kutzick; A Flörcken; T Voit
Journal:  Hum Mol Genet       Date:  2001-01-01       Impact factor: 6.150

Review 6.  The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members (review).

Authors:  H G Joost; B Thorens
Journal:  Mol Membr Biol       Date:  2001 Oct-Dec       Impact factor: 2.857

7.  Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome.

Authors:  D Wang; P Kranz-Eble; D C De Vivo
Journal:  Hum Mutat       Date:  2000-09       Impact factor: 4.878

8.  Autosomal dominant glut-1 deficiency syndrome and familial epilepsy.

Authors:  K Brockmann; D Wang; C G Korenke; A von Moers; Y Y Ho; J M Pascual; K Kuang; H Yang; L Ma; P Kranz-Eble; J Fischbarg; F Hanefeld; D C De Vivo
Journal:  Ann Neurol       Date:  2001-10       Impact factor: 10.422

9.  The efficacy of the ketogenic diet-1998: a prospective evaluation of intervention in 150 children.

Authors:  J M Freeman; E P Vining; D J Pillas; P L Pyzik; J C Casey; L M Kelly
Journal:  Pediatrics       Date:  1998-12       Impact factor: 7.124

10.  EEG features of glut-1 deficiency syndrome.

Authors:  Arpad von Moers; Knut Brockmann; Dong Wang; Christoph G Korenke; Peter Huppke; Darryl C De Vivo; Folker Hanefeld
Journal:  Epilepsia       Date:  2002-08       Impact factor: 5.864

  10 in total
  9 in total

1.  Crystal structure of the human glucose transporter GLUT1.

Authors:  Dong Deng; Chao Xu; Pengcheng Sun; Jianping Wu; Chuangye Yan; Mingxu Hu; Nieng Yan
Journal:  Nature       Date:  2014-05-18       Impact factor: 49.962

2.  GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.

Authors:  Yvonne G Weber; Alexander Storch; Thomas V Wuttke; Knut Brockmann; Judith Kempfle; Snezana Maljevic; Lucia Margari; Christoph Kamm; Susanne A Schneider; Stephan M Huber; Arnulf Pekrun; Robert Roebling; Guiscard Seebohm; Saisudha Koka; Camelia Lang; Eduard Kraft; Dragica Blazevic; Alberto Salvo-Vargas; Michael Fauler; Felix M Mottaghy; Alexander Münchau; Mark J Edwards; Anna Presicci; Francesco Margari; Thomas Gasser; Florian Lang; Kailash P Bhatia; Frank Lehmann-Horn; Holger Lerche
Journal:  J Clin Invest       Date:  2008-06       Impact factor: 14.808

Review 3.  Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).

Authors:  Toni S Pearson; Cigdem Akman; Veronica J Hinton; Kristin Engelstad; Darryl C De Vivo
Journal:  Curr Neurol Neurosci Rep       Date:  2013-04       Impact factor: 5.081

Review 4.  Inborn errors of metabolism and motor disturbances in children.

Authors:  A García-Cazorla; N I Wolf; M Serrano; B Pérez-Dueñas; M Pineda; J Campistol; E Fernández-Alvarez; J Colomer; S DiMauro; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2009-10       Impact factor: 4.982

5.  Genetic Identification in Early Onset Parkinsonism among Norwegian Patients.

Authors:  Emil K Gustavsson; Joanne Trinh; Marna McKenzie; Stephanie Bortnick; Maria Skaalum Petersen; Matthew J Farrer; Jan O Aasly
Journal:  Mov Disord Clin Pract       Date:  2017-05-23

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

7.  Molecular Dynamics Simulations of the Human Glucose Transporter GLUT1.

Authors:  Min-Sun Park
Journal:  PLoS One       Date:  2015-04-28       Impact factor: 3.240

8.  Total Intravenous Anesthesia in GLUT1 Deficiency Syndrome Patient: A Case Report.

Authors:  Jan Kloka; Stefanie Kranepuhl; Kai Zacharowski; Florian Jürgen Raimann
Journal:  Am J Case Rep       Date:  2019-05-05

Review 9.  Episodic Ataxias: Faux or Real?

Authors:  Paola Giunti; Elide Mantuano; Marina Frontali
Journal:  Int J Mol Sci       Date:  2020-09-05       Impact factor: 5.923

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.