Episodic ataxia type 2 manifests as epileptiform electroencephalographic activity with no epileptic attacks in two family members

Author:

Kaido Misako1,Furuta Mitsuru2,Nakamori Masayuki2,Yuasa Yoshihito1,Takahashi Masanori P.2

Affiliation:

1. Department of Neurology, Sakai City Medical Center

2. Department of Neurology, Osaka University Graduate School of Medicine

Publisher

Societas Neurologica Japonica

Subject

Clinical Neurology

Reference12 articles.

1. 2) NEUROMUSCULAR DISEASE CENTER. Episodic Ataxias [Internet]. St. Louis, MO USA: Washington University; 2015 Nov 6. [cited 2015 Nov 8]. Available from: http://neuromuscular.wustl.edu/

2. 3) Gene Reviews® Episodic Ataxia Type 2 [Internet]. Seattle (WA) USA: University of Washington; 2015 Oct 15. [cited 2015 Nov 8]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1501/

3. 4) OMIM® #108500 EPISODIC ATAXIA, TYPE 2; EA2 [Internet]. Baltimore, MD USA: the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine; 2014 Apr 29. [cited 2015 Nov 8]. Available from: http://omim.org/entry/108500

4. 5) Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996;87:543-552.

5. 6) Baloh RW, Yue Q, Furman JM, et al. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p. Ann Neurol 1997;41:8-16.

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