Literature DB >> 12887436

Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretations.

Kette D Valente1, Joaquina Q Andrade, Rosi M Grossmann, Fernando Kok, Cintia Fridman, Célia P Koiffmann, Maria J Marques-Dias.   

Abstract

PURPOSE: This study aimed to evaluate the sensitivity of the EEG in Angelman syndrome (AS), to verify the age at onset of suggestive EEGs and to study EEG patterns, analyzing variations and comparing our findings with nomenclature previously used.
METHODS: Seventy EEG and 15 V-EEGs of 26 patients were analyzed. Suggestive EEG patterns of AS were classified in delta pattern (DP), theta pattern (TP), and posterior discharges (PDs). Generic terms were used to simplify the analysis.
RESULTS: Suggestive EEGs were observed in 25 (96.2%) patients. DP occurred in 22 patients with four variants-hypsarrhythmic-like: irregular, high-amplitude, generalized delta activity (DA) with multifocal epileptiform discharges (EDs); slow variant: regular, high-amplitude, generalized DA with rare EDs; ill-defined slow spike-and-wave: regular, high-amplitude, generalized DA with superimposed EDs characterizing a slow wave, with notched appearance; triphasic-like: rhythmic, moderate-amplitude DA over anterior regions with superimposed EDs. TP was observed in eight patients, as generalized or over the posterior regions. PDs were seen in 19 patients as runs of sharp waves or runs of high-amplitude slow waves with superimposed EDs. TP was the only age-related pattern (younger than 8 years) and observed only in patients with deletion. In 15 patients who had an EEG before the clinical diagnosis, 60% had a suggestive tracing.
CONCLUSIONS: Although some EEG descriptions are not very detailed, and every author describes findings in a slightly different manner, obviously a common denominator must exist. In this context, EEG seems to be a very sensitive method for the diagnosis of AS, offering an opportunity to corroborate this etiologic diagnosis. Conversely, we do not believe that these patterns may be accounted as specific, except for the delta pattern, which seems to be extremely unusual in other syndromes. Other EEG patterns observed in AS, such as theta activity and PDs, occur in a wide variety of disorders. Nonetheless, their importance for the EEG diagnosis of AS is supported by the fact that they are associated with other features and may be helpful in a proper clinical setting.

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Year:  2003        PMID: 12887436     DOI: 10.1046/j.1528-1157.2003.66502.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  16 in total

1.  Revisiting epilepsy and the electroencephalogram patterns in Angelman syndrome.

Authors:  Marcio Leyser; Patricia Sola Penna; Alexandre Cardozo de Almeida; Marcio Moacyr Vasconcelos; Osvaldo J M Nascimento
Journal:  Neurol Sci       Date:  2014-01-07       Impact factor: 3.307

Review 2.  Sleep Disturbances in Neurodevelopmental Disorders.

Authors:  Althea Robinson-Shelton; Beth A Malow
Journal:  Curr Psychiatry Rep       Date:  2016-01       Impact factor: 5.285

3.  Electrophysiological Phenotype in Angelman Syndrome Differs Between Genotypes.

Authors:  Joel Frohlich; Meghan T Miller; Lynne M Bird; Pilar Garces; Hannah Purtell; Marius C Hoener; Benjamin D Philpot; Michael S Sidorov; Wen-Hann Tan; Maria-Clemencia Hernandez; Alexander Rotenberg; Shafali S Jeste; Michelle Krishnan; Omar Khwaja; Joerg F Hipp
Journal:  Biol Psychiatry       Date:  2019-01-19       Impact factor: 13.382

Review 4.  Angelman syndrome and melatonin: What can they teach us about sleep regulation.

Authors:  Daniella Buonfiglio; Daniel L Hummer; Ariel Armstrong; John Christopher Ehlen; Jason P DeBruyne
Journal:  J Pineal Res       Date:  2020-10-11       Impact factor: 13.007

Review 5.  Epilepsy in patients with Angelman syndrome.

Authors:  Agata Fiumara; Annarita Pittalà; Mariadonatella Cocuzza; Giovanni Sorge
Journal:  Ital J Pediatr       Date:  2010-04-16       Impact factor: 2.638

6.  Cannabidiol attenuates seizures and EEG abnormalities in Angelman syndrome model mice.

Authors:  Bin Gu; Manhua Zhu; Madison R Glass; Marie Rougié; Viktoriya D Nikolova; Sheryl S Moy; Paul R Carney; Benjamin D Philpot
Journal:  J Clin Invest       Date:  2019-12-02       Impact factor: 14.808

7.  A 19-month-old boy with decreased sleep and a distinctive electroencephalogram pattern.

Authors:  Julie Baughn; Erik K St Louis
Journal:  J Clin Sleep Med       Date:  2021-07-01       Impact factor: 4.324

8.  Angelman syndrome presenting with a rare seizure type in a patient with 15q11.2 deletion: a case report.

Authors:  Jagath C Ranasinghe; Damitha Chandradasa; Sanjaya Fernando; Uditha Kodithuwakku; D E N Mandawala; Vajira H W Dissanayake
Journal:  J Med Case Rep       Date:  2015-06-16

9.  Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome.

Authors:  Glenda Lassi; Lorenzo Priano; Silvia Maggi; Celina Garcia-Garcia; Edoardo Balzani; Nadia El-Assawy; Marco Pagani; Federico Tinarelli; Daniela Giardino; Alessandro Mauro; Jo Peters; Alessandro Gozzi; Graziano Grugni; Valter Tucci
Journal:  Sleep       Date:  2016-03-01       Impact factor: 5.849

10.  Delta power robustly predicts cognitive function in Angelman syndrome.

Authors:  Lauren M Ostrowski; Elizabeth R Spencer; Lynne M Bird; Ronald Thibert; Robert W Komorowski; Mark A Kramer; Catherine J Chu
Journal:  Ann Clin Transl Neurol       Date:  2021-05-28       Impact factor: 4.511

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