Home LiteratureArticle Details
PMID: 8614512 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Familial migraine with vertigo and essential tremor.

Neurology ·Vol. 46 ·No. 2 ·1996-02-00 ·Pages 458-60

Baloh RW, Foster CA, Yue Q, Nelson SF

Abstract

We report a family with dominantly inherited migraine headaches, episodic vertigo, and essential tremor. All symptoms improved with the use of acetazolamide. Linkage analysis ruled out linkage to markers on chromosome 19p, known to be linked to the genetic defect in families with the clinically similar syndromes of hemiplegic migraine and periodic ataxia. This genetic heterogeneity of migraine syndromes could result from defects in a family of genes coding proteins with similar properties.

MeSH Terms
Adult Chromosomes, Human, Pair 19 DNA/blood,isolation & purification DNA, Satellite/genetics Female Genes, Dominant Genetic Linkage Genetic Markers Humans Male Migraine Disorders/complications,genetics Pedigree Polymerase Chain Reaction Tremor/complications,genetics Vertigo/complications,genetics
Chemicals
DNA, Satellite Genetic Markers DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Baloh R W
Department of Neurology, UCLA School of Medicine, Los Angeles, CA 90095-1769, USA.
Foster C A
Yue Q
Nelson S F
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1996-02-00
Pages
458-60
Language
English
Region
United States
NLM ID
0401060
Subset
IM
Grants
NIA NIH HHS · NIA AG 09693 · United States
NIDCD NIH HHS · NIDCD DC 01404 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]