PubMed · 3387179
[Hyperexplexia: the startle disease].
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.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
I Melki, E Rizkallah, C Akatcherian. 1988. [Hyperexplexia: the startle disease].. https://pubmed.ncbi.nlm.nih.gov/3387179/
Cite the original work for its findings. Save a collection to share your selection of sources.