Literature DB >> 16764981

Catatonic stupor superimposed on hereditary spinocerebellar degeneration resolved with electroconvulsive therapy.

Kazumasa Suzuki1, Kae Itou, Takehisa Takano, Nobuhiko Harada, Shuichi Awata, Hiroo Matsuoka.   

Abstract

We report a 58-year-old woman with catatonic stupor superimposed on hereditary spinocerebellar degeneration (SCD) and psychotic depression. The catatonia and psychotic depression resolved with 11 sessions of electroconvulsive therapy (ECT). Early recognition of catatonia during the course of SCD is important for timely administration of ECT.

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Year:  2006        PMID: 16764981     DOI: 10.1016/j.pnpbp.2006.04.026

Source DB:  PubMed          Journal:  Prog Neuropsychopharmacol Biol Psychiatry        ISSN: 0278-5846            Impact factor:   5.067


  2 in total

1.  Electroconvulsive therapy resolves cortical inhibition and manneristic omissions in a chronic catatonic patient.

Authors:  T Dresler; A S Giani; C Reinsberger; P Scheuerpflug; G Stöber; A J Fallgatter
Journal:  J Neural Transm (Vienna)       Date:  2010-09-01       Impact factor: 3.575

2.  Major Depressive Disorder Complicated with Spinocerebellar Ataxia: Report of 2 Cases.

Authors:  Nagahisa Okamoto; Masafumi Ogawa; Yoshiko Murata; Kota Sakamoto; Tatsuya Nagai; Maki Yamada; Teruhiko Higuchi
Journal:  Case Rep Neurol       Date:  2010-05-12
  2 in total

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