Literature DB >> 6689893

Familial startle disease (hyperexplexia). Electrophysiologic studies.

O N Markand, B P Garg, D D Weaver.   

Abstract

Six affected members from a family of 15 patients with familial startle disease (hyperexplexia) underwent extensive electrophysiologic evaluation. The most marked abnormality consisted of prominent C response 60 to 75 ms after median and peroneal nerve stimulation. The somatosensory evoked responses were also relatively high in amplitude. These findings suggest that hyperactive long-loop reflexes may constitute the physiologic basis of startle disease.

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Year:  1984        PMID: 6689893     DOI: 10.1001/archneur.1984.04050130077028

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


  4 in total

1.  Hyperexplexia or stiff baby syndrome.

Authors:  C Tohier; J C Roze; A David; M F Veccierini; P Renaud; A Mouzard
Journal:  Arch Dis Child       Date:  1991-04       Impact factor: 3.791

2.  Stiff man syndrome: neurophysiological findings in eight patients.

Authors:  H M Meinck; K Ricker; P J Hülser; M Solimena
Journal:  J Neurol       Date:  1995-02       Impact factor: 4.849

3.  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

4.  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
  4 in total

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