Major and minor form of hereditary hyperekplexia
- PMID: 12210885
- DOI: 10.1002/mds.10168
Major and minor form of hereditary hyperekplexia
Abstract
Hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses. Within the disorder two clinical forms can be distinguished. The major form is characterized by continuous generalized stiffness in the first year of life and an exaggerated startle reflex, accompanied by temporary generalized stiffness and falls, whereas in the minor form only excessive startle and hypnic jerks have been described. Mutations in the gene encoding the alpha-1 subunit of the glycine receptor (GLRA1) are responsible for the major form of hyperekplexia but no mutation was detected in patients with the minor form in the large Dutch pedigree originally described by Suhren and colleagues. Here we describe the genetic analysis of the GLRA1 gene of two English families in which both forms of hyperekplexia were present. Mutation analysis revealed no genetic defect in the GLRA1 gene in patients carrying either the minor or major forms. This is further evidence that the minor form of hyperekplexia is seldom due to a genetic defect in the GLRA1 gene.
Copyright 2002 Movement Disorder Society
Similar articles
-
[Familial hyperekplexia: startle disease. Clinical, electrophysiological and genetic study of a family].Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):447-50. Rev Neurol (Paris). 1996. PMID: 8944241 Review. French.
-
Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation.Pediatr Neurol. 2012 Feb;46(2):89-93. doi: 10.1016/j.pediatrneurol.2011.11.008. Pediatr Neurol. 2012. PMID: 22264702
-
The novel hyperekplexia allele GLRA1(S267N) affects the ethanol site of the glycine receptor.Eur J Hum Genet. 2008 Feb;16(2):223-8. doi: 10.1038/sj.ejhg.5201958. Epub 2007 Nov 28. Eur J Hum Genet. 2008. PMID: 18043720
-
[Startle disease: growing rigid with fear].Ned Tijdschr Geneeskd. 1995 Sep 23;139(38):1940-3. Ned Tijdschr Geneeskd. 1995. PMID: 7477535 Dutch.
-
Startle syndromes.Lancet Neurol. 2006 Jun;5(6):513-24. doi: 10.1016/S1474-4422(06)70470-7. Lancet Neurol. 2006. PMID: 16713923 Review.
Cited by
-
Hereditary hyperekplexia caused by novel mutations of GLRA1 in Turkish families.Mol Diagn. 2004;8(3):151-5. doi: 10.1007/BF03260058. Mol Diagn. 2004. PMID: 15771552
-
Synaptopathies: synaptic dysfunction in neurological disorders - A review from students to students.J Neurochem. 2016 Sep;138(6):785-805. doi: 10.1111/jnc.13713. Epub 2016 Sep 8. J Neurochem. 2016. PMID: 27333343 Free PMC article. Review.
-
Sporadic Hyperekplexia Plus Syndrome.J Pediatr Neurosci. 2017 Jan-Mar;12(1):36-39. doi: 10.4103/jpn.JPN_170_16. J Pediatr Neurosci. 2017. PMID: 28553377 Free PMC article.
-
Startle Disease: New Molecular Insights into an Old Neurological Disorder.Neuroscientist. 2023 Dec;29(6):767-781. doi: 10.1177/10738584221104724. Epub 2022 Jun 25. Neuroscientist. 2023. PMID: 35754344 Free PMC article. Review.
-
Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease.Neurobiol Dis. 2013 Apr;52:137-49. doi: 10.1016/j.nbd.2012.12.001. Epub 2012 Dec 10. Neurobiol Dis. 2013. PMID: 23238346 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources