Literature DB >> 12907280

Ataxia with vitamin E deficiency and severe dystonia: report of a case.

Agathe Roubertie1, Brigitte Biolsi, François Rivier, Véronique Humbertclaude, Renée Cheminal, Bernard Echenne.   

Abstract

Mutation of the gene for alpha-tocopherol transfer protein causes ataxia with isolated vitamin E deficiency, a disorder usually stabilized or improved after vitamin E supplementation. Dystonia has rarely been described in ataxia with isolated vitamin E deficiency (AVED) patients. We present the case of a young boy with AVED, whose neurological and extra-neurological cardinal symptoms of the disease improved after vitamin E supplementation but who progressively developed generalized dystonia.

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Year:  2003        PMID: 12907280     DOI: 10.1016/s0387-7604(03)00054-8

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  8 in total

1.  Ataxia with Vitamin E Deficiency with Predominant Cervical Dystonia.

Authors:  Swati Pradeep; Tarek Ali; Zain Guduru
Journal:  Mov Disord Clin Pract       Date:  2019-12-30

Review 2.  Ataxia with vitamin E deficiency: update of molecular diagnosis.

Authors:  I Di Donato; S Bianchi; A Federico
Journal:  Neurol Sci       Date:  2010-05-13       Impact factor: 3.307

3.  Epilepsy in a patient with ataxia caused by vitamin E deficiency.

Authors:  Kai Ivar Müller; Svein Ivar Bekkelund
Journal:  BMJ Case Rep       Date:  2011-05-03

Review 4.  Assessment of patients with isolated or combined dystonia: an update on dystonia syndromes.

Authors:  Victor S C Fung; H A Jinnah; Kailash Bhatia; Marie Vidailhet
Journal:  Mov Disord       Date:  2013-06-15       Impact factor: 10.338

5.  Ataxia with Vitamin E Deficiency May Present with Cervical Dystonia.

Authors:  Andrew E Becker; Wendy Vargas; Toni S Pearson
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2016-05-17

Review 6.  More Than Ataxia: Hyperkinetic Movement Disorders in Childhood Autosomal Recessive Ataxia Syndromes.

Authors:  Toni S Pearson
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2016-07-16

Review 7.  Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Authors:  Aymane Bouzidi; Hicham Charoute; Majida Charif; Ghita Amalou; Mostafa Kandil; Abdelhamid Barakat; Guy Lenaers
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

Review 8.  Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options.

Authors:  Malco Rossi; Bettina Balint; Patricio Millar Vernetti; Kailash P Bhatia; Marcelo Merello
Journal:  Mov Disord Clin Pract       Date:  2018-07-03
  8 in total

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