Literature DB >> 11952078

Hyperekplexia in a girl with posterior fossa malformations.

Jatinder S Goraya1, Durlabh Shah, Banani Poddar.   

Abstract

Hyperekplexia is a rare clinical syndrome of pathologic startle response to unexpected stimuli such as sound or touch. The majority of cases are familial. Sporadic cases of hyperekplexia have also been reported, mostly in association with brainstem pathology. We describe a girl with sporadic hyperekplexia secondary to previously unreported cerebellar pathology. Her symptomatology was predominantly unilateral, being ipsilateral to the cerebellar involvement. This type of presentation, which may be termed hemihyperekplexia, has not been described before. Response to clonazepam was good but showed diurnal variations. The case is being reported for its unusual features.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11952078     DOI: 10.1177/088307380201700213

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  5 in total

1.  The role of tonic glycinergic conductance in cerebellar granule cell signalling and the effect of gain-of-function mutation.

Authors:  Catherine McLaughlin; John Clements; Ana-Maria Oprişoreanu; Sergiy Sylantyev
Journal:  J Physiol       Date:  2019-04-02       Impact factor: 5.182

2.  A new Purkinje cell antibody (anti-Ca) associated with subacute cerebellar ataxia: immunological characterization.

Authors:  Sven Jarius; Klaus P Wandinger; Sigrun Horn; Heike Heuer; Brigitte Wildemann
Journal:  J Neuroinflammation       Date:  2010-03-12       Impact factor: 8.322

Review 3.  'Medusa head ataxia': the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: Anti-PKC-gamma, anti-GluR-delta2, anti-Ca/ARHGAP26 and anti-VGCC.

Authors:  S Jarius; B Wildemann
Journal:  J Neuroinflammation       Date:  2015-09-17       Impact factor: 8.322

4.  A confusing coincidence: neonatal hypoglycemic seizures and hyperekplexia.

Authors:  Nihat Demir; Murat Doğan; Sanem Yılmaz; Erdal Peker; Keziban Bulan; Oğuz Tuncer
Journal:  Case Rep Med       Date:  2014-03-24

5.  A novel syndrome of lethal familial hyperekplexia associated with brain malformation.

Authors:  Mohammed Zein Seidahmed; Mustafa A Salih; Omer B Abdulbasit; Meeralebbae Shaheed; Khalid Al Hussein; Abeer M Miqdad; Abdullah K Al Rasheed; Anas M Alazami; Ibrahim A Alorainy; Fowzan S Alkuraya
Journal:  BMC Neurol       Date:  2012-10-27       Impact factor: 2.474

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.