Locus for familial migrainous vertigo disease maps to chromosome 5q35

Annals of Otology, Rhinology and Laryngology

Volumn 118, Issue 9, 2009, Pages 670-676

  Bahmad Jr , Fayez ^a,b,c   DePalma, Steven R ^a   Merchant, Saumil N ^b   Bezerra, Roberta L ^c   Oliveira, Carlos A ^c   Seidman, Christine E ^a   Seidman, Jonathan G ^a  

^a HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^b MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^c UNIVERSITY OF BRASILIA   (Brazil)

Author keywords

Familial disease; Gene; Linkage study; Migraine; Vertigo

Indexed keywords

ADULT; AGED; ARTICLE; AUDIOMETRY; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 5; CLINICAL ARTICLE; CONTROLLED STUDY; EPISODIC VERTIGO; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; HEARING LOSS; HUMAN; MALE; MICROSATELLITE MARKER; MIGRAINE; PERCEPTION DEAFNESS; PRESBYACUSIS; PRIORITY JOURNAL; VESTIBULAR TEST;

EID: 70349451523     PISSN: 00034894     EISSN: None     Source Type: Journal    
DOI: 10.1177/000348940911800912     Document Type: Article

References (31)

1. Kayan A, Hood JD. Neuro-otological manifestations of migraine. Brain 1984;107:1123-1142
2. Neuhauser H, Leopold M, von Brevern M, Arnold G, Lempert T. The interrelations of migraine, vertigo, and migrainous vertigo. Neurology 2001;56:436-441
3. Baloh RW. Neurotology of migraine. Headache 1997;37:615-621
4. Eggers SD. Migraine-related vertigo: diagnosis and treatment. Curr Pain Headache Rep 2007;11:217-226
5. Maione A. Migraine-related vertigo: diagnostic criteria and prophylactic treatment. Laryngoscope 2006;116:1782-1786 (Pubitemid 44511361)
6. Bikhazi P, Jackson C, Ruckenstein MJ. Efficacy of anti-migrainous therapy in the treatment of migraine-associated dizziness. Am J Otol 1997;18:350-354 (Pubitemid 27239946)
7. Dieterich M, Brandt T. Episodic vertigo related to migraine (90 cases): vestibular migraine? J Neurol 1999;246:883-892
8. Cass SP, Furman JM, Ankerstjerne K, Balaban C, Yetiser S, Aydogan B. Migraine-related vestibulopathy. Ann Otol Rhinol Laryngol 1997;106:182-189
9. Marcus DA, Kapelewski C, Rudy TE, Jacob RG, Furman JM. Diagnosis of migrainous vertigo: validity of a structured interview. Med Sci Monit 2004;10:CR197-CR201. (Pubitemid 38787628)
10. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Headache Classification Committee of the International Headache Society. Cephalalgia 1988;8(suppl 7):1-96.
11. Oliveira CA, Bezerra RL, Araújo MF, Almeida VF, Messias CI. Meniere's syndrome and migraine: incidence in one family. Ann Otol Rhinol Laryngol 1997;106:823-829 (Pubitemid 27459029)
12. Oliveira CA, Ferrari I, Messias CI. Occurrence of familial Meniere's syndrome and migraine in Brasília. Ann Otol Rhinol Laryngol 2002;111:229-236 (Pubitemid 34233349)
13. Bezerra RL. Meniere's syndrome and migraine: familial incidence and genetic transmission [Dissertation]. Brasília, Brazil: Brasília University, 2002.
14. Haines JL, Korf BR, Morton CC, Seidman CE, Seidman JG, Smith DR, eds. Current protocols in human genetics. Newark, NJ: John Wiley and Sons, 2008.
15. Song L, DePalma SR, Kharlap M, et al. Novel locus for an inherited cardiomyopathy maps to chromosome 7. Circulation 2006;113:2186-2192 (Pubitemid 43755141)
16. Wessman M, Kallela M, Kaunisto MA, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet 2002;70:652-662 (Pubitemid 34177920)
17. Cader ZM, Noble-Topham S, Dyment DA, et al. Significant linkage to migraine with aura on chromosome 11q24. Hum Mol Genet 2003;12:2511-2517 (Pubitemid 37220415)
18. Russo L, Mariotti P, Sangiorgi E, et al. A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes. Am J Hum Genet 2005;76:327-333 (Pubitemid 40129558)
19. Kaunisto MA, Tikka PJ, Kallela M, et al. Chromosome 19p13 loci in Finnish migraine with aura families. Am J Med Genet B Neuropsychiatr Genet 2005;132B:85-89 (Pubitemid 40066202)
20. von Brevern M, Ta N, Shankar A, et al. Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4. Headache 2006;46:1136-1141 (Pubitemid 43992583)
21. Lee H, Jen JC, Wang H, et al. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Hum Mol Genet 2006;15:251-258 (Pubitemid 43125979)
22. O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 1995;11:402-408
23. Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984;36:460-465
24. Cottingham RW Jr, Idury RM, Schäffer AA. Faster sequential genetic linkage computations. Am J Hum Genet 1993;53:252-263 (Pubitemid 23313755)
25. Kong A, Gudbjartsson DF, Sainz J, et al. A high-resolution recombination map of the human genome. Nat Genet 2002;31:241-247 (Pubitemid 34887588)
26. Karolchik D, Kuhn RM, Baertsch R, et al. The UCSC Genome Browser Database: 2008 update. Nucleic Acids Res 2008;36:D773-D779.
27. Kuritzky A, Toglia UJ, Thomas D. Vestibular function in migraine. Headache 1981;21:110-112
28. Olsson JE. Neurotologic findings in basilar migraine. Laryngoscope 1991;101:1-41.
29. Fedorova ML. Vestibular syndrome in migraine [in Russian]. Klin Med (Mosk) 1970;48:70-76
30. Parker W. Migraine and the vestibular system in adults. Am J Otol 1991;12:25-34.
31. Committee on Hearing and Equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease. American Academy of Otolaryngology-Head and Neck Foundation, Inc. Otolaryngol Head Neck Surg 1995;113:181-185