Familial clustering and genetic heterogeneity in Meniere's disease

Clinical Genetics

Volumn 85, Issue 3, 2014, Pages 245-252

  Requena, T ^a   Espinosa Sanchez, J M ^a,b   Cabrera, S ^a   Trinidad, G ^c   Soto Varela, A ^d   Santos Perez, S ^d   Teggi, R ^e   Perez, P ^f   Batuecas Caletrio, A ^g   Fraile, J ^h   Aran, I ⁱ   Martin, E ^j   Benitez, J ^k   Perez Fernandez N ^l   Lopez Escamez, J A ^a,m  

^a UNIVERSITY OF GRANADA   (Spain)

^b HOSPITAL SAN AGUSTÍN   (Spain)

^c Department of Otorhinolaryngology   (Spain)

^d HOSPITAL CLÍNICO UNIVERSITARIO   (Spain)

^e SAN RAFFAELE HOSPITAL   (Italy)

^f HOSPITAL DE CABUEÑES   (Spain)

^g HOSPITAL UNIVERSITARIO DE SALAMANCA   (Spain)

^h HOSPITAL UNIVERSITARIO MIGUEL SERVET   (Spain)

ⁱ Complexo Hospitalario de Pontevedra ^*  (Spain)

^j HOSPITAL UNIVERSITARIO DE GETAFE   (Spain)

^k HOSPITAL UNIVERSITARIO DE GRAN CANARIA DR NEGRÍN   (Spain)

^l UNIVERSITY CLINIC OF NAVARRA   (Spain)

^m HOSPITAL DE PONIENTE   (Spain)

more..

Author keywords

Anticipation; Autosomal dominant; Endolymphatic hydrops; Familial Meniere's disease; Sensorineural hearing loss; Twins; Vertigo

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CLUSTER ANALYSIS; DIZYGOTIC TWINS; EPISODIC VERTIGO; EXTRACHROMOSOMAL INHERITANCE; FAMILY HISTORY; FEMALE; GENETIC HETEROGENEITY; GENOME IMPRINTING; HEADACHE; HEARING IMPAIRMENT; HUMAN; MAJOR CLINICAL STUDY; MALE; MENIERE DISEASE; MIDDLE AGED; MIGRAINE; MONOZYGOTIC TWINS; MULTICENTER STUDY (TOPIC); ONSET AGE; PRIORITY JOURNAL; RECURRENCE RISK; RECURRENT DISEASE; AGED; COHORT ANALYSIS; FAMILY; GENETIC PREDISPOSITION; GENETICS; ITALY; PEDIGREE; PREVALENCE; SPAIN; TWINS;

ADULT; AGE OF ONSET; AGED; COHORT STUDIES; FAMILY; FEMALE; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ITALY; MALE; MENIERE DISEASE; MIDDLE AGED; PEDIGREE; PREVALENCE; SPAIN; TWINS;

EID: 84893006604     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12150     Document Type: Article

References (40)

1. Paparella MM. Pathology of Meniere's disease. Ann Otol Rhinol Laryngol Suppl 1984: 112: 31-35.
2. Sajjadi H, Paparella MM. Meniere's disease. Lancet 2008: 372: 406-414.
3. Merchant SN, Adams JC, Nadol JB Jr. Pathophysiology of Meniere's syndrome: are symptoms caused by endolymphatic hydrops? Otol Neurotol 2005: 26: 74-81.
4. Friberg U, Stahle J, Svedberg A. The natural course of Meniere's disease. Acta Otolaryngol Suppl 1984: 406: 72-77.
5. Alexander TH, Harris JP. Current epidemiology of Meniere's syndrome. Otolaryngol Clin North Am 2010: 43: 965-970.
6. Gazquez I, Soto-Varela A, Aran I et al. High prevalence of systemic autoimmune diseases in patients with Meniere's disease. PLoS One 2011: 6: e26759.
7. Lopez-Escamez JA, Viciana D, Garrido-Fernandez P. Impact of bilaterality and headache on health-related quality of life in Meniere's disease. Ann Otol Rhinol Laryngol 2009: 118: 409-416.
8. Levo H, Stephens D, Poe D et al. EuroQol 5D quality of life in Meniere's disorder can be explained with symptoms and disabilities. Int J Rehabil Res 2012: 35: 197-202.
9. Stahle J, Friberg U, Svedberg A. Long-term progression of Meniere's disease. Acta Otolaryngol Suppl 1991: 485: 78-83.
10. House JW, Doherty JK, Fisher LM et al. Meniere's disease: prevalence of contralateral ear involvement. Otol Neurotol 2006: 27: 355-361.
11. Kitahara M. Bilateral aspects of Meniere's disease: Meniere's disease with bilateral fluctuant hearing loss. Acta Otolaryngol Suppl 1991: 485: 74-77.
12. Clemmens C, Ruckenstein M. Characteristics of patients with unilateral and bilateral Meniere's disease. Otol Neurotol 2012: 33: 1266-1269.
13. Vrabec JT. Genetic investigations of Meniere's disease. Otolaryngol Clin North Am 2010: 43: 1121-1132.
14. Morrison AW, Bailey ME, Morrison GA. Familial Meniere's disease: clinical and genetic aspects. J Laryngol Otol 2009: 123: 29-37.
15. Klar J, Frykholm C, Friberg U et al. A Meniere's disease gene linked to chromosome 12p12.3. Am J Med Genet B Neuropsychiatr Genet 2006: 141B: 463-467.
16. Arweiler-Harbeck D, Horsthemke B, Jahnke K et al. Genetic aspects of familial Meniere's disease. Otol Neurotol 2011: 32: 695-700.
17. Birgerson L, Gustavson KH, Stahle J. Familial Meniere's disease: a genetic investigation. Am J Otol 1987: 8: 323-326.
18. Gazquez I, Requena T, Espinosa JM et al. Genetic and clinical heterogeneity in Meniere's disease. Autoimmun Rev 2012: 11: 925-926.
19. Gabrikova D, Frykholm C, Friberg U et al. Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association. J Hum Genet 2010: 55: 834-837.
20. Morrison AW, Mowbray JF, Williamson R et al. On genetic and environmental factors in Meniere's disease. Am J Otol 1994: 15: 35-39.
21. Perez-Garrigues H, Lopez-Escamez JA, Perez P et al. Time course of episodes of definitive vertigo in Meniere's disease. Arch Otolaryngol Head Neck Surg 2008: 134: 1149-1154.
22. Belinchon A, Perez-Garrigues H, Tenias JM. Evolution of symptoms in Meniere's disease. Audiol Neurootol 2012: 17: 126-132.
23. Committee on Hearing and Equilibrium. Guidelines for the diagnosis and evaluation of therapy in Meniere's disease. American Academy of Otolaryngology-Head and Neck Foundation, Inc. Otolaryngol Head Neck Surg 1995: 113: 181-185.
24. Morales Angulo C, Gomez Castellanos R, Garcia Mantilla J et al. Epidemiology of Meniere's disease in Cantabria. Acta Otorrinolaringol Esp 2003: 54: 601-605.
25. Wladislavosky-Waserman P, Facer GW, Mokri B et al. Meniere's disease: a 30-year epidemiologic and clinical study in Rochester, Mn, 1951-1980. Laryngoscope 1984: 94: 1098-1102.
26. Wickramaratne P, Hodge S. Estimation of sibling recurrence-risk ratio under single ascertainment in two-child families. Am J Hum Genet 2001: 68: 807-812.
27. Klockars T, Kentala E. Inheritance of Meniere's disease in the Finnish population. Arch Otolaryngol Head Neck Surg 2007: 133: 73-77.
28. Lempert T, Olesen J, Furman J et al. Vestibular migraine: diagnostic criteria. J Vestib Res 2012: 22: 167-172.
29. Risch N. Linkage strategies for genetically complex traits I. Multilocus models. Am J Hum Genet 1990: 46: 222-228.
30. Veltman JA, Brunner HG. De novo mutations in human genetic disease. Nat Rev Genet 2012: 13: 565-575.
31. Rybicki BA, Elston RC. The relationship between the sibling recurrence-risk ratio and genotype relative risk. Am J Hum Genet 2000: 66: 593-604.
32. Oliveira CA, Ferrari I, Messias CI. Occurrence of familial Meniere's syndrome and migraine in Brasilia. Ann Otol Rhinol Laryngol 2002: 111: 229-236.
33. Cha YH, Kane MJ, Baloh RW. Familial clustering of migraine, episodic vertigo, and Meniere's disease. Otol Neurotol 2008: 29: 93-96.
34. Hietikko E, Kotimaki J, Kentala E et al. Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings. Genet Med 2011: 13: 415-420.
35. Kokotas H, Petersen MB, Willems PJ. Mitochondrial deafness. Clin Genet 2007: 71: 379-391.
36. Morrison AW. Anticipation in Meniere's disease. J Laryngol Otol 1995: 109: 499-502.
37. Pollak A. Otosclerosis associated with Meniere's disease: a histological study. Adv Otorhinolaryngol 2007: 65: 50-52.
38. Eza-Nunez P, Manrique-Rodriguez M, Perez-Fernandez N. Otosclerosis among patients with dizziness. Rev Laryngol Otol Rhinol 2010: 131: 199-206.
39. Brown MR. The factor of heredity in labyrinthine deafness and paroxysmal vertigo; Meniere's syndrome. Ann Otol Rhinol Laryngol 1949: 58: 665-670.
40. O'Roak BJ, Deriziotis P, Lee C et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet 2011: 43: 585-589.