Literature DB >> 3387179

[Hyperexplexia: the startle disease].

I Melki1, E Rizkallah, C Akatcherian.   

Abstract

A case of hyperexplexia is reported in a newborn. Hyperexplexia or "startle disease" is very uncommon and is of autosomal dominant transmission. Clinical features consist in particular physical features during the neonatal period and subsequently in an abnormal startle reaction; the electromyogram shows particular patterns.

Entities:  

Mesh:

Year:  1988        PMID: 3387179

Source DB:  PubMed          Journal:  Pediatrie        ISSN: 0031-4021


  1 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

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.