Literature DB >> 11319492

[Psychiatric disorders in juvenile myoclonic epilepsy].

P Gélisse1, P Genton, J C Samuelian, P Thomas, M Bureau.   

Abstract

Mild personality problems have been described in patients with juvenile myoclonic epilepsy (JME), but clinical practice shows that JME can be diagnosed in patients with more or less severe psychiatric disorders (PD). The presence in JME patients of personality disorders has been described repeatedly, but never quantified. We thus decided to evaluate, using the DSM IV, the current prevalence and types of PD in a large series of consecutive, newly referred patients with JME. Among 170 consecutive JME cases referred to two departments of epileptology (Marseilles and Nice) between 1981 and 1998 (66 males, 104 females; aged 11.7-70; mean+/-SD 32.4+/-10.4 follow-up 12.7+/-10 [0.5-52]), we found 45 patients (26.5p.100) with PD. According to the DSM IV, they could be classified as severe mental retardation (main diagnosis) (one case); pervasive developmental disorders (2 cases); tic disorder (1 case); enuresis (1 case); psychotic disorders (5 cases, including schizophrenia paranoid type (1 case), disorganized type (1 case), delusional disorder (1 case), unspecified (2 cases)); depressive disorders (3 cases); generalized anxiety (6 cases); anorexia nervosa (2 cases); personality disorders (24 cases, including borderline personality (11 cases), dependent personality (5 cases), histrionic personality (2 cases), obsessive-compulsive personality (1 case), not specified (5 cases)). Sudden unexplained death occurred in 2 cases (borderline personality and pervasive developmental disorder not otherwise specified, respectively) and death due to pneumonia in 1 cases (anorexia). Although uncommonly severe cases of JME may have been selected in our referral centers, it appears that JME may be associated with PD. Comparatively mild personality disorders are the most common finding, and may be part of the clinical picture to some extent, while severe PD are less common, and probably coincidental. The presence of PD does not exclude the diagnosis of JME, and PD may represent a further challenge in the comprehensive care of these patients.

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Year:  2001        PMID: 11319492

Source DB:  PubMed          Journal:  Rev Neurol (Paris)        ISSN: 0035-3787            Impact factor:   2.607


  4 in total

1.  Structural brain abnormalities in juvenile myoclonic epilepsy patients: volumetry and voxel-based morphometry.

Authors:  Woo Suk Tae; Seung Bong Hong; Eun Yun Joo; Sun Jung Han; Jae-Wook Cho; Dae Won Seo; Jong-Min Lee; In Young Kim; Hong Sik Byun; Sun I Kim
Journal:  Korean J Radiol       Date:  2006 Jul-Sep       Impact factor: 3.500

2.  Cortical thickness abnormality in juvenile myoclonic epilepsy.

Authors:  Woo Suk Tae; Sun Hyung Kim; Eun Yun Joo; Sun Jung Han; In Yong Kim; Sun I Kim; Jong-Min Lee; Seung Bong Hong
Journal:  J Neurol       Date:  2008-01-31       Impact factor: 4.849

Review 3.  Cognitive Function in Genetic Generalized Epilepsies: Insights From Neuropsychology and Neuroimaging.

Authors:  Corey Ratcliffe; Britta Wandschneider; Sallie Baxendale; Pamela Thompson; Matthias J Koepp; Lorenzo Caciagli
Journal:  Front Neurol       Date:  2020-03-10       Impact factor: 4.003

4.  The association between temperament features and childhood traumas in patients with juvenile myoclonic epilepsy

Authors:  Alişan Burak Yaşar; Ceyhun Sayman; Serap Erdoğan Taycan; Yilmaz Çetinkaya; Anil Gündüz; Hülya Tireli
Journal:  Turk J Med Sci       Date:  2020-08-26       Impact factor: 0.973

  4 in total

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