Literature DB >> 33163569

Hemiplegic Migraine in Glut1 Deficiency Syndrome and Paroxysmal Dyskinesia at Ketogenic Diet Induction: Case Report and Literature Review.

Janina Gburek-Augustat1, Anja Heinze2, Rami Abou Jamra2, Andreas Merkenschlager1.   

Abstract

BACKGROUND: A rare symptom of Glut1 deficiency syndrome (Glut1 DS) is hemiplegic migraine (HM). CASE: We report a patient with Glut1 DS with a mild phenotype. His leading symptom was HM. As an unusual complication of the initiation of a ketogenic diet (KD), our patient developed paroxysmal nonkinesigenic dyskinesia. Paroxysmal dyskinesia occurred first and exclusively at the initiation of KD. LITERATURE REVIEW: There are a few case reports for HM in Glut1 DS. All patients had additional neurological symptoms. Regarding central nervous system symptoms such as paroxysmal dyskinesia triggered by KD, we found only 1 other case report. DISCUSSION: HM is part of the symptom complex of Glut1 DS and can be effectively treated by KD. Paroxysmal dyskinesia trigged by the initiation of KD should not lead to the discontinuation of the diet in Glut1 DS.
© 2020 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  Glut1 DS, hemiplegic migraine, paroxysmal nonkinesigenic dyskinesia, paroxysmal hemiparesis, side effect of KD

Year:  2020        PMID: 33163569      PMCID: PMC7604676          DOI: 10.1002/mdc3.13087

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN: 2330-1619


  19 in total

1.  Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.

Authors:  Y G Weber; C Kamm; A Suls; J Kempfle; K Kotschet; R Schüle; T V Wuttke; S Maljevic; J Liebrich; T Gasser; A C Ludolph; W Van Paesschen; L Schöls; P De Jonghe; G Auburger; H Lerche
Journal:  Neurology       Date:  2011-08-10       Impact factor: 9.910

2.  Glut1 deficiency and alternating hemiplegia of childhood.

Authors:  M Rotstein; J Doran; H Yang; P M Ullner; K Engelstad; D C De Vivo
Journal:  Neurology       Date:  2009-12-08       Impact factor: 9.910

3.  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

4.  Basal ganglia injury as a complication of the ketogenic diet.

Authors:  Jay C Erickson; Bahman Jabbari; Marc P Difazio
Journal:  Mov Disord       Date:  2003-04       Impact factor: 10.338

5.  Sodium valproate inhibits glucose transport and exacerbates Glut1-deficiency in vitro.

Authors:  Hei Yi Wong; Tsui Shan Chu; Janice Ching Lai; Kwok Pui Fung; Tai Fai Fok; Tatsuya Fujii; Yuan Yuan Ho
Journal:  J Cell Biochem       Date:  2005-11-01       Impact factor: 4.429

6.  Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively.

Authors:  J Klepper; H Scheffer; B Leiendecker; E Gertsen; S Binder; M Leferink; C Hertzberg; A Näke; T Voit; M A Willemsen
Journal:  Neuropediatrics       Date:  2005-10       Impact factor: 1.947

Review 7.  GLUT1 deficiency syndrome 2013: current state of the art.

Authors:  Valentina De Giorgis; Pierangelo Veggiotti
Journal:  Seizure       Date:  2013-07-26       Impact factor: 3.184

8.  A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood.

Authors:  Claudia M Weller; Wilhelmina G Leen; Brian G R Neville; John S Duncan; Boukje de Vries; Marije A Geilenkirchen; Joost Haan; Erik-Jan Kamsteeg; Michel D Ferrari; Arn M J M van den Maagdenberg; Michèl A A P Willemsen; Hans Scheffer; Gisela M Terwindt
Journal:  Cephalalgia       Date:  2014-05-13       Impact factor: 6.292

9.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

Review 10.  The clinical and genetic heterogeneity of paroxysmal dyskinesias.

Authors:  Alice R Gardiner; Fatima Jaffer; Russell C Dale; Robyn Labrum; Roberto Erro; Esther Meyer; Georgia Xiromerisiou; Maria Stamelou; Matthew Walker; Dimitri Kullmann; Tom Warner; Paul Jarman; Mike Hanna; Manju A Kurian; Kailash P Bhatia; Henry Houlden
Journal:  Brain       Date:  2015-11-23       Impact factor: 13.501

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