Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000036.xml
Laryngorhinootologie 2021; 100(06): 472-476
DOI: 10.1055/a-1463-3536
DOI: 10.1055/a-1463-3536
Der interessante Fall
Klarer Fall von Morbus Menière?
Obvious case of Morbus Menière?Bei langjähriger Schwindelsymptomatik kann auch bei initial neurologisch unauffälligem Status eine Erkrankung des Zentralnervensystems zugrunde liegen. Bei therapieresistenten Verläufen und dem Auftreten von neurologischen Beschwerden sollte daher die Diagnose im Verlauf überprüft werden, insbesondere bevor invasive therapeutische Maßnahmen eingeleitet werden.
Publication History
Article published online:
09 April 2021
© 2021. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
Literatur
- 1 Bauer P, Stevanin G, Beetz C. et al. Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds. Journal of Neurology, Neurosurgery & Psychiatry 2010; 81: 1229-1232
- 2 Bürk K, Strzelczyk A, Reif PS. et al. Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13). International Journal of Neuroscience 2013; 123: 278-282
- 3 Figueroa KP, Minassian NA, Stevanin G. et al. KCNC3: phenotype, mutations, channel biophysics – a study of 260 familial ataxia patients. Human mutation 2010; 31: 191-196
- 4 Herman-Bert A, Stevanin G, Netter JC. et al. Mapping of spinocerebellar ataxia 13 to chromosome 19q13. 3-q13. 4 in a family with autosomal dominant cerebellar ataxia and mental retardation. The American Journal of Human Genetics 2000; 67: 229-235
- 5 Irie T, Matsuzaki Y, Sekino Y. et al. Kv3. 3 channels harbouring a mutation of spinocerebellar ataxia type 13 alter excitability and induce cell death in cultured cerebellar Purkinje cells. The Journal of physiology 2014; 592: 229-247
- 6 Issa FA, Mazzochi C, Mock AF. et al. Spinocerebellar ataxia type 13 mutant potassium channel alters neuronal excitability and causes locomotor deficits in zebrafish. Journal of Neuroscience 2011; 31: 6831-6841
- 7 Issa FA, Mock AF, Sagasti A. et al. Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development. Disease models & mechanisms 2012; 5: 921-929
- 8 Lopez-Escamez JA, Carey J, Chung WH. et al. Diagnostic criteria for Meniere's disease. J Vestib Res 2015; 25: 1-7
- 9 Middlebrooks JC, Nick HS, Subramony S. et al. Mutation in the kv3. 3 voltage-gated potassium channel causing spinocerebellar ataxia 13 disrupts sound-localization mechanisms. PloS one 2013; 8: e76749
- 10 Mock AF, Richardson JL, Hsieh JY. et al. Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3. 3 channels. BMC neuroscience 2010; 11: 99
- 11 Syrbe S, Hedrich UB, Riesch E. et al. De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy. Nature genetics 2015; 47: 393-399
- 12 Waters M, Fee D, Figueroa K. et al. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?. Neurology 2005; 65: 1111-1113
- 13 Waters MF. Spinocerebellar ataxia type 13. GeneReviews® 2020 [Internet]
- 14 Waters MF, Minassian NA, Stevanin G. et al. Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes. Nature genetics 2006; 38: 447-451