Literature DB >> 6830476

Hyperekplexia.

T W Kurczynski.   

Abstract

Hyperekplexia is a hereditary neurologic disorder manifested by an exaggerated startle response, generalized muscular rigidity, and prominent nocturnal myoclonus. The distinctive features of this syndrome constitute an unusual clinical entity that is easily mistaken for other disorders. The study of a family provided additional data on various aspects of this condition. The proband was 3 months old when he was referred for persistent generalized stiffness since birth; this stiffness was associated with an exaggerated startle response and intermittent apnea. Similar symptoms in infancy and prominent nocturnal myoclonus with an excessive startle response in adulthood were described in other family members for five generations. Various features of the disorder indicate a relationship to the syndrome of the "jumping Frenchmen of Maine," latah, miryachit, and other unusual startle reactions.

Entities:  

Mesh:

Year:  1983        PMID: 6830476     DOI: 10.1001/archneur.1983.04050040076015

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  10 in total

Review 1.  Hyperekplexia in neonates.

Authors:  V Praveen; S K Patole; J S Whitehall
Journal:  Postgrad Med J       Date:  2001-09       Impact factor: 2.401

2.  Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes.

Authors:  T M Lewis; L G Sivilotti; D Colquhoun; R M Gardiner; R Schoepfer; M Rees
Journal:  J Physiol       Date:  1998-02-15       Impact factor: 5.182

Review 3.  Movement disorder emergencies.

Authors:  Steven J Frucht
Journal:  Curr Neurol Neurosci Rep       Date:  2005-07       Impact factor: 5.081

Review 4.  Movement disorder emergencies.

Authors:  Kathleen L Poston; Steven J Frucht
Journal:  J Neurol       Date:  2008-08       Impact factor: 4.849

5.  The glycinergic system in human startle disease: a genetic screening approach.

Authors:  Jeff S Davies; Seo-Kyung Chung; Rhys H Thomas; Angela Robinson; Carrie L Hammond; Jonathan G L Mullins; Eloisa Carta; Brian R Pearce; Kirsten Harvey; Robert J Harvey; Mark I Rees
Journal:  Front Mol Neurosci       Date:  2010-03-23       Impact factor: 5.639

6.  Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.

Authors:  S G Ryan; M J Dixon; M A Nigro; K A Kelts; O N Markand; J C Terry; R Shiang; J J Wasmuth; P O'Connell
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

Review 7.  Glycine receptor mouse mutants: model systems for human hyperekplexia.

Authors:  Natascha Schaefer; Georg Langlhofer; Christoph J Kluck; Carmen Villmann
Journal:  Br J Pharmacol       Date:  2013-11       Impact factor: 8.739

8.  Hyperekplexia and stiff-baby syndrome: an identical neurological disorder?

Authors:  G Cioni; E Biagioni; P Bottai; A M Castellacci; P B Paolicelli
Journal:  Ital J Neurol Sci       Date:  1993-03

9.  Transient neuromotor phenotype in transgenic spastic mice expressing low levels of glycine receptor beta-subunit: an animal model of startle disease.

Authors:  L Becker; B Hartenstein; J Schenkel; J Kuhse; H Betz; H Weiher
Journal:  Eur J Neurosci       Date:  2000-01       Impact factor: 3.386

10.  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

  10 in total

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