Literature DB >> 1622521

Hyperekplexia and sudden neonatal death.

M A Nigro1, H C Lim.   

Abstract

Fifteen patients with hyperekplexia were identified in 3 families; diagnostic clinical characteristics were defined which allowed for early recognition and treatment. During the first 24 hours of life, spontaneous apnea and sluggish feeding effort were observed. After the first 24 hours, surviving infants exhibited the hyperekplexic startle response to nose tapping. This startle response is characterized by sudden muscular rigidity, feeding-induced oropharyngeal incoordination, and poor air exchange often with apnea, persisting with repetitive nose tapping. Untreated infants experienced recurring apnea until 1 year of age. Three of 15 patients died unexpectedly during the neonatal period. Patients treated with clonazepam (0.1-0.2 mg/kg/day) had no serious apneic episodes and startle reflexes were diminished. The pathophysiologic mechanism for hyperekplexia remains obscure. Electroencephalographic studies were consistently normal. The response to and tolerance of benzodiazepines are striking in newborns and infants and suggest an aberrant central nervous system reflex as the etiology; therefore, hyperekplexia should be considered in the evaluation of neonates and infants with apnea, aspiration pneumonia, episodic muscular rigidity, hyperexcitability, and near-miss sudden infant death syndrome. The need for immediate monitoring of at-risk infants, observation for signs of hyperekplexia, and initiation of clonazepam in these patients are emphasized. Hyperekplexic startle response to nose tapping should be included in the routine examination of all newborns.

Entities:  

Mesh:

Year:  1992        PMID: 1622521     DOI: 10.1016/0887-8994(92)90073-8

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  11 in total

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Authors:  N Fejerman
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8.  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

9.  Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.

Authors:  Eloisa Carta; Seo-Kyung Chung; Victoria M James; Angela Robinson; Jennifer L Gill; Nathalie Remy; Jean-François Vanbellinghen; Cheney J G Drew; Sophie Cagdas; Duncan Cameron; Frances M Cowan; Mireria Del Toro; Gail E Graham; Adnan Y Manzur; Amira Masri; Serge Rivera; Emmanuel Scalais; Rita Shiang; Kate Sinclair; Catriona A Stuart; Marina A J Tijssen; Grahame Wise; Sameer M Zuberi; Kirsten Harvey; Brian R Pearce; Maya Topf; Rhys H Thomas; Stéphane Supplisson; Mark I Rees; Robert J Harvey
Journal:  J Biol Chem       Date:  2012-06-14       Impact factor: 5.157

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

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