Is benign myoclonic epilepsy of infancy truly idiopathic and generalized?

نویسندگان

  • Christian M Korff
  • Pierre Jallon
  • Agustina Lascano
  • Christoph Michel
  • Margitta Seeck
  • Charles-Antoine Haenggeli
چکیده

Benign myoclonic epilepsy of infancy is recognized as a generalized and idiopathic epilepsy by the International League Against Epilepsy. Unprovoked and reflex seizures have been reported in these patients. We describe a child diagnosed with benign myoclonic epilepsy of infancy, whose strictly unilateral and localized reflex myoclonias broaden the clinical spectrum of this idiopathic and generalized epileptic syndrome, and raise interrogations about its underlying pathophysiological mechanisms. [Published with video sequences].

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Idiopathisch generalisierte Epilepsien: Klinische Syndrome und Pathogenese

Idiopathic Generalized Epilepsies: Clinical Syndromes and Pathogenesis. Most kinds of idiopathic generalized epilepsies (IGE) such as juvenile myoclonic epilepsy (JME), absence epilepsy in infancy (CAE), myoclonic absence epilepsy (MAE), juvenile absence epilepsy

متن کامل

Benign myoclonic epilepsy in infancy followed by childhood absence epilepsy

Benign myoclonic epilepsy in infancy (BMEI) is a rare syndrome included among idiopathic generalized epilepsies (IGE) and syndromes with age-related onset. Recently, it has been shown that a few patients with BMEI later had other epilepsy types mainly IGE but never childhood absence epilepsy (CAE). We report a patient who at 11 months of age showed isolated myoclonic jerks occurring several tim...

متن کامل

Epidemiology of idiopathic generalized epilepsies.

Idiopathic generalized epilepsies (IGEs) are a relatively new category of disorders defined by strict clinical and electroencephalogram (EEG) features proposed by the International League Against Epilepsy (ILAE) classification of epileptic syndromes. IGEs are usually easy to diagnose when clinical and EEG data are collected, but epilepsy is not synonymous with epileptic syndrome. So far, IGEs a...

متن کامل

ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies.

Benign familial neonatal convulsions 20q13 KCNQ2 (1–3) 8q24 KCNQ3 (4,5) Childhood absence epilepsy 8q24 ? (6,7) AD Juvenile myoclonic epilepsy 6p21 ? (8–14) 5q14 ? (15,16) 5q34 GABRA1 (17) Adolescent-onset idiopathic generalized epilepsies 8p12 ? (14,18) 18q12 ? (14) 5p ? (14) Idiopathic generalized epilepsy 3q26 ? (19) 14q23 ? (19) 2q36 ? (19) Benign familial infantile convulsions 19q ? (20) 1...

متن کامل

Epilepsy syndromes in infancy.

An increasing number of infantile epilepsy syndromes have been recognized. However, a significant number of infants (children aged 1-24 months) do not fit in any of the currently used subcategories. This article reviews the clinical presentation, electroencephalographic findings, evolution, and management of the following entities: early infantile epileptic encephalopathy, early myoclonic epile...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Epileptic disorders : international epilepsy journal with videotape

دوره 11 2  شماره 

صفحات  -

تاریخ انتشار 2009