Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Search research articles

Related Experiment Videos

The benign partial nonrolandic epilepsies.

P Lerman¹, S Kivity

¹Pediatric Seizure Clinic and EEG Laboratory, Beilinson Medical Center, Petah Tikva, Israel.

Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society

|July 1, 1991

Summary

This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by

Same author

Tuftsin-phosphorylcholine (TPC) equally effective to methylprednisolone in ameliorating lupus nephritis in a mice model.

Clinical and experimental immunology·2018

Same author

The clinical phenotype of patients positive for antibodies to myositis and myositis-related disorders.

Clinical rheumatology·2018

Same author

Hydroxychloroquine desensitization, an effective method to overcome hypersensitivity-a multicenter experience.

Lupus·2017

Same author

Neuropsychiatric SLE: from animal model to human.

Lupus·2017

Same author

Anti-citrullinated-protein-antibody-specific intravenous immunoglobulin attenuates collagen-induced arthritis in mice.

Clinical and experimental immunology·2015

Same author

Low ALT blood levels predict long-term all-cause mortality among adults. A historical prospective cohort study.

European journal of internal medicine·2014

Same journal

Surface EEG to Identify Cognitive Motor Dissociation After Acute Brain Injury.

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society·2026

Same journal

The Physics and Physiology of Electrical Stimulation of the Brain.

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society·2026

Same journal

Neurophysiology in Postanoxic Encephalopathy: Pathophysiology, Prognosis, and Treatment.

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society·2026

Same journal

A Review on the Functional Connectivity of the Human Opercular Cortex.

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society·2026

Same journal

Surgical Aspects of Opercular Epilepsies.

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society·2026

Same journal

Cost-Effectiveness of EEG Monitoring in Hypoxic-Ischemic Brain Injury After Cardiac Arrest.

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society·2026

See all related articles

Benign partial epilepsies, beyond rolandic epilepsy, are genetically determined childhood disorders. These conditions, often diagnosed after 18 months, typically present with brief seizures and resolve before adulthood.

Area of Science:

Pediatric Neurology
Epileptology
Clinical Neuroscience

Background:

Rolandic epilepsy is the sole recognized benign epileptic syndrome.
Other forms of benign partial epilepsy exist in neurologically healthy children.
These syndromes are age-dependent and genetically influenced.

Purpose of the Study:

To detail non-rolandic benign partial epilepsies.
To review the current literature on these conditions.
To highlight their characteristics and diagnostic criteria.

Main Methods:

Literature review of benign partial epilepsy syndromes.
Analysis of clinical features, EEG findings, and genetic factors.
Comparison of rolandic epilepsy with other benign forms.

Related Experiment Videos

Main Results:

Several benign partial epilepsies are identified, including benign occipital, frontal, and psychomotor epilepsy.
These epilepsies typically feature brief, infrequent seizures responsive to medication and self-remitting.
Normal EEG background with sleep-activated spikes is common; Landau-Kleffner syndrome is sometimes included.

Conclusions:

Benign partial epilepsies represent a spectrum of childhood-onset seizure disorders.
Early identification and understanding of these syndromes are crucial for appropriate management.
Further research into genetic and clinical aspects can refine diagnostic and therapeutic approaches.