Literature DB >> 27093447

GNAL mutation in isolated laryngeal dystonia.

Gregory G Putzel1, Tania Fuchs1, Giovanni Battistella1, Estee Rubien-Thomas1, Steven J Frucht1, Andrew Blitzer1,2, Laurie J Ozelius3, Kristina Simonyan1,4.   

Abstract

BACKGROUND: Up to 12% of patients with laryngeal dystonia report a familial history of dystonia, pointing to involvement of genetic factors. However, its genetic causes remain unknown.
METHOD: Using Sanger sequencing, we screened 57 patients with isolated laryngeal dystonia for mutations in known dystonia genes TOR1A (DYT1), THAP1 (DYT6), TUBB4A (DYT4), and GNAL (DYT25). Using functional MRI, we explored the influence of the identified mutation on brain activation during symptomatic task production.
RESULTS: We identified 1 patient with laryngeal dystonia who was a GNAL mutation carrier. When compared with 26 patients without known mutations, the GNAL carrier had increased activity in the fronto-parietal cortex and decreased activity in the cerebellum.
CONCLUSIONS: Our data show that GNAL mutation may represent one of the rare causative genetic factors of isolated laryngeal dystonia. Exploratory evidence of distinct neural abnormalities in the GNAL carrier may suggest the presence of divergent pathophysiological cascades underlying this disorder.
© 2016 International Parkinson and Movement Disorder Society. © 2016 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  Dystonia; genetic factors; neuroimaging; spasmodic dysphonia

Mesh:

Substances:

Year:  2016        PMID: 27093447      PMCID: PMC4933312          DOI: 10.1002/mds.26502

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  34 in total

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