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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.490 Epilepsy .
C10.228.140.490.360 Epilepsies, Partial .
C10.228.140.490.370 Epilepsy, Benign Neonatal .
C10.228.140.490.375 Epilepsy, Generalized .
C10.228.140.490.375.130 Epilepsies, Myoclonic .
C10.228.140.490.375.130.670 Myoclonic Epilepsy, Juvenile .
C10.228.140.490.375.260 Epilepsy, Absence .
C10.228.140.490.375.290 Epilepsy, Tonic-Clonic .
C10.228.140.490.493 Epileptic Syndromes .
C10.228.140.490.493.063 Epilepsies, Myoclonic .
C10.228.140.490.493.063.670 Myoclonic Epilepsy, Juvenile .
C10.228.140.490.493.125 Epilepsy, Absence .
C10.597 Neurologic Manifestations .
C10.597.742 Seizures .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.614 Infant, Newborn, Diseases .
C16.614.258 Epilepsy, Benign Neonatal .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.742 Seizures .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Epilepsy, Tonic-Clonic .
Convulsions, Grand Mal .
Cryptogenic Tonic-Clonic Epilepsy .
Epilepsy, Tonic-Clonic, Cryptogenic .
Epilepsy, Tonic-Clonic, Familial .
Epilepsy, Tonic-Clonic, Symptomatic .
Familial Tonic-Clonic Epilepsy .
Seizure Disorder, Grand Mal .
Seizure Disorder, Major Motor .
Symptomatic Tonic-Clonic Epilepsy .
Tonic Clonic Convulsions .
Tonic-Clonic Convulsion Disorder .
Tonic-Clonic Convulsion Syndrome .
Tonic-Clonic Seizure Disorder .
Tonic-Clonic Seizure Syndrome .
Convulsion Disorder, Tonic-Clonic .
Convulsion Disorders, Tonic-Clonic .
Convulsion Syndrome, Tonic-Clonic .
Convulsion Syndromes, Tonic-Clonic .
Convulsion, Grand Mal .
Convulsion, Tonic Clonic .
Convulsions, Tonic Clonic .
Cryptogenic Tonic Clonic Epilepsy .
Cryptogenic Tonic-Clonic Epilepsies .
Disorder, Tonic-Clonic Convulsion .
Disorder, Tonic-Clonic Seizure .
Disorders, Tonic-Clonic Convulsion .
Disorders, Tonic-Clonic Seizure .
Epilepsies, Cryptogenic Tonic-Clonic .
Epilepsies, Familial Tonic-Clonic .
Epilepsies, Symptomatic Tonic-Clonic .
Epilepsies, Tonic-Clonic .
Epilepsy, Cryptogenic Tonic-Clonic .
Epilepsy, Familial Tonic-Clonic .
Epilepsy, Symptomatic Tonic-Clonic .
Epilepsy, Tonic Clonic .
Familial Tonic Clonic Epilepsy .
Familial Tonic-Clonic Epilepsies .
Grand Mal Convulsion .
Grand Mal Convulsions .
Grand Mal Epilepsy .
Major Epilepsies .
Major Epilepsy .
Seizure Disorder, Tonic-Clonic .
Seizure Disorders, Tonic-Clonic .
Seizure Syndrome, Tonic-Clonic .
Seizure Syndromes, Tonic-Clonic .
Symptomatic Tonic Clonic Epilepsy .
Symptomatic Tonic-Clonic Epilepsies .
Syndrome, Tonic-Clonic Convulsion .
Syndrome, Tonic-Clonic Seizure .
Syndromes, Tonic-Clonic Convulsion .
Syndromes, Tonic-Clonic Seizure .
Tonic Clonic Convulsion .
Tonic Clonic Convulsion Disorder .
Tonic Clonic Convulsion Syndrome .
Tonic Clonic Seizure Disorder .
Tonic Clonic Seizure Syndrome .
Tonic-Clonic Convulsion Disorders .
Tonic-Clonic Convulsion Syndromes .
Tonic-Clonic Epilepsies .
Tonic-Clonic Epilepsies, Cryptogenic .
Tonic-Clonic Epilepsies, Familial .
Tonic-Clonic Epilepsies, Symptomatic .
Tonic-Clonic Epilepsy .
Tonic-Clonic Epilepsy, Cryptogenic .
Tonic-Clonic Epilepsy, Familial .
Tonic-Clonic Epilepsy, Symptomatic .
Tonic-Clonic Seizure Disorders .
Tonic-Clonic Seizure Syndromes .
Epilepsy, Grand Mal .
Epilepsy, Major .
Grand Mal Seizure Disorder .
Major Motor Seizure Disorder .
Seizure Disorder, Tonic Clonic .
A generalized seizure disorder characterized by recurrent major motor seizures. The initial brief tonic phase is marked by trunk flexion followed by diffuse extension of the trunk and extremities. The clonic phase features rhythmic flexor contractions of the trunk and limbs, pupillary dilation, elevations of blood pressure and pulse, urinary incontinence, and tongue biting. This is followed by a profound state of depressed consciousness (post-ictal state) which gradually improves over minutes to hours. The disorder may be cryptogenic, familial, or symptomatic (caused by an identified disease process). (From Adams et al., Principles of Neurology, 6th ed, p329) .
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Epilepsy, Absence .
Absence Seizure Disorder .
Childhood Absence Epilepsy .
Epilepsy Juvenile Absence .
Epilepsy, Absence, Atypical .
Epilepsy, Petit Mal .
Juvenile Absence Epilepsy .
Pykno-Epilepsy .
Seizure Disorder, Absence .
Absence Epilepsies, Childhood .
Absence Epilepsies, Juvenile .
Absence Epilepsy .
Absence Epilepsy, Childhood .
Absence Epilepsy, Juvenile .
Absence Seizure Disorders .
Childhood Absence Epilepsies .
Epilepsies, Childhood Absence .
Epilepsies, Juvenile Absence .
Epilepsy Juvenile Absences .
Epilepsy, Childhood Absence .
Epilepsy, Juvenile Absence .
Juvenile Absence Epilepsies .
Juvenile Absence, Epilepsy .
Juvenile Absences, Epilepsy .
Minor Epilepsies .
Minor Epilepsy .
Petit Mal Epilepsies .
Petit Mal, Akinetic .
Pykno Epilepsy .
Pykno-Epilepsies .
Pyknolepsies .
Seizure Disorders, Absence .
Akinetic Petit Mal .
Pyknolepsy .
Petit Mal Epilepsy .
Epilepsy, Minor .
EPILEPSY, PETIT MAL .
A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736) .
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Epilepsies, Partial .
Amygdalo-Hippocampal Epilepsy .
Benign Focal Epilepsy, Childhood .
Benign Occipital Epilepsy .
Benign Occipital Epilepsy, Childhood .
Childhood Benign Focal Epilepsy .
Childhood Benign Occipital Epilepsy .
Epilepsy, Benign Occipital .
Epilepsy, Localization-Related .
Epilepsy, Partial .
Occipital Lobe Epilepsy .
Partial Seizures, Simple, Consciousness Preserved .
Rhinencephalic Epilepsy .
Seizure Disorder, Focal .
Subclinical Seizure .
Uncinate Seizures .
Abdominal Epilepsies .
Amygdalo-Hippocampal Epilepsies .
Benign Occipital Epilepsies .
Digestive Epilepsies .
Disorders, Focal Seizure .
Disorders, Partial Seizure .
Epilepsies, Abdominal .
Epilepsies, Amygdalo-Hippocampal .
Epilepsies, Benign Occipital .
Epilepsies, Digestive .
Epilepsies, Focal .
Epilepsies, Gelastic .
Epilepsies, Localization-Related .
Epilepsies, Occipital Lobe .
Epilepsies, Rhinencephalic .
Epilepsies, Simple Partial .
Epilepsy, Abdominal .
Focal Epilepsies .
Focal Epilepsy .
Focal Seizure Disorders .
Gelastic Epilepsies .
Lobe Epilepsy, Occipital .
Localization-Related Epilepsies .
Localization-Related Epilepsy .
Occipital Epilepsies, Benign .
Occipital Epilepsy, Benign .
Occipital Lobe Epilepsies .
Partial Epilepsies .
Partial Epilepsies, Simple .
Partial Seizure Disorders .
Partial Seizures, Simple .
Rhinencephalic Epilepsies .
Seizure Disorders, Focal .
Seizure Disorders, Partial .
Seizure, Subclinical .
Seizure, Uncinate .
Seizures, Simple Partial .
Seizures, Subclinical .
Seizures, Uncinate .
Simple Partial Epilepsies .
Subclinical Seizures .
Epilepsy, Focal .
Epilepsy, Simple Partial .
Seizure Disorder, Partial .
Abdominal Epilepsy .
Digestive Epilepsy .
Focal Seizure Disorder .
Partial Epilepsy .
Gelastic Epilepsy .
Partial Seizure Disorder .
Simple Partial Seizures .
EPILEPSY, GENERALIZED SECONDARY .
EPILEPSY, LOCALIZATION-RELATED .
EPILEPSY, PARTIAL .
Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317) .
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Seizures .
Atonic Absence Seizures .
Atonic Seizures .
Clonic Seizures .
Complex Partial Seizures .
Convulsion, Non-Epileptic .
Generalized Absence Seizures .
Generalized Tonic-Clonic Seizures .
Myoclonic Seizures .
Non-Epileptic Seizures .
Nonepileptic Seizures .
Partial Seizures .
Petit Mal Convulsion .
Seizures, Auditory .
Seizures, Clonic .
Seizures, Epileptic .
Seizures, Gustatory .
Seizures, Olfactory .
Seizures, Somatosensory .
Seizures, Tonic .
Seizures, Tonic-Clonic .
Seizures, Vertiginous .
Seizures, Vestibular .
Seizures, Visual .
Single Seizure .
Tonic Seizures .
Tonic-Clonic Seizures .
Absence Seizure .
Absence Seizure, Atonic .
Absence Seizure, Generalized .
Absence Seizures, Atonic .
Absence Seizures, Generalized .
Atonic Absence Seizure .
Atonic Seizure .
Auditory Seizure .
Auditory Seizures .
Clonic Seizure .
Complex Partial Seizure .
Convulsion .
Convulsion, Non Epileptic .
Convulsion, Petit Mal .
Convulsions, Non-Epileptic .
Convulsive Seizure .
Epileptic Seizure .
Focal Seizure .
Focal Seizures .
Generalized Absence Seizure .
Generalized Seizure .
Generalized Seizures .
Generalized Tonic Clonic Seizures .
Generalized Tonic-Clonic Seizure .
Gustatory Seizure .
Gustatory Seizures .
Motor Seizure .
Motor Seizures .
Myoclonic Seizure .
Non Epileptic Seizures .
Non-Epileptic Convulsion .
Non-Epileptic Convulsions .
Non-Epileptic Seizure .
Nonepileptic Seizure .
Olfactory Seizure .
Olfactory Seizures .
Partial Seizure .
Partial Seizure, Complex .
Partial Seizures, Complex .
Seizure .
Seizure, Absence .
Seizure, Atonic .
Seizure, Atonic Absence .
Seizure, Auditory .
Seizure, Clonic .
Seizure, Complex Partial .
Seizure, Convulsive .
Seizure, Epileptic .
Seizure, Focal .
Seizure, Generalized .
Seizure, Generalized Absence .
Seizure, Generalized Tonic-Clonic .
Seizure, Gustatory .
Seizure, Jacksonian .
Seizure, Motor .
Seizure, Myoclonic .
Seizure, Non-Epileptic .
Seizure, Nonepileptic .
Seizure, Olfactory .
Seizure, Partial .
Seizure, Sensory .
Seizure, Single .
Seizure, Somatosensory .
Seizure, Tonic .
Seizure, Tonic-Clonic .
Seizure, Vertiginous .
Seizure, Vestibular .
Seizure, Visual .
Seizures, Atonic .
Seizures, Atonic Absence .
Seizures, Complex Partial .
Seizures, Generalized Absence .
Seizures, Generalized Tonic-Clonic .
Seizures, Myoclonic .
Seizures, Non-Epileptic .
Seizures, Nonepileptic .
Seizures, Partial .
Seizures, Single .
Seizures, Tonic Clonic .
Sensory Seizure .
Sensory Seizures .
Single Seizures .
Somatosensory Seizure .
Somatosensory Seizures .
Tonic Clonic Seizures .
Tonic Seizure .
Tonic-Clonic Seizure .
Tonic-Clonic Seizure, Generalized .
Tonic-Clonic Seizures, Generalized .
Vertiginous Seizure .
Vertiginous Seizures .
Vestibular Seizure .
Vestibular Seizures .
Visual Seizure .
Visual Seizures .
Convulsions .
Convulsive Seizures .
Jacksonian Seizure .
Seizures, Convulsive .
Seizures, Focal .
Seizures, Generalized .
Seizures, Motor .
Seizures, Sensory .
Epileptic Seizures .
Absence Seizures .
Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or "seizure disorder." .
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Myoclonic Epilepsy, Juvenile .
Adolescent Myoclonic Epilepsy .
Epilepsy, Myoclonic Juvenile .
Impulsive Petit Mal Epilepsy .
JME (Juvenile Myoclonic Epilepsy) .
Janz Impulsive Petit Mal .
Janz Juvenile Myoclonic Epilepsy .
Juvenile Myoclonic Epilepsy of Janz .
Myoclonic Epilepsy, Adolescent .
Myoclonic Epilepsy, Juvenile, 1 .
Panayiotopoulos Syndrome .
Petit Mal, Impulsive .
Petit Mal, Impulsive, Janz .
Adolescent Myoclonic Epilepsies .
Epilepsies, Adolescent Myoclonic .
Epilepsies, Juvenile Myoclonic .
Epilepsies, Myoclonic Juvenile .
Epilepsy, Adolescent Myoclonic .
Epilepsy, Juvenile Myoclonic .
JMEs (Juvenile Myoclonic Epilepsy) .
Juvenile Epilepsies, Myoclonic .
Juvenile Epilepsy, Myoclonic .
Juvenile Myoclonic Epilepsies .
Myoclonic Epilepsies, Adolescent .
Myoclonic Epilepsies, Juvenile .
Myoclonic Juvenile Epilepsies .
Myoclonic Juvenile Epilepsy .
Panayiotopoulos Syndromes .
Petit Mals, Impulsive .
Epilepsy, Myoclonic, Juvenile .
Impulsive Petit Mal, Janz .
Janz Syndrome .
Juvenile Myoclonic Epilepsy .
A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323) .
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Epilepsy, Benign Neonatal .
Benign Familial Infantile Convulsions .
Benign Familial Infantile Convulsions Syndrome .
Benign Familial Neonatal Convulsions .
Benign Familial Neonatal Epilepsy .
Benign Familial Neonatal-Infantile Seizures .
Benign Infantile Familial Convulsions .
Benign Neonatal Convulsions .
Benign Neonatal Epilepsy .
Benign Neonatal Epilepsy, Nonfamilial .
Benign Neonatal Non-Familial Convulsions .
Benign Neonatal Nonfamilial Epilepsy .
Benign Non-Familial Neonatal Convulsions .
Convulsions Benign Familial Neonatal .
Convulsions, Benign Familial Infantile, 1 .
Convulsions, Benign Familial Infantile, 3 .
Convulsions, Benign Neonatal, Familial .
Convulsions, Benign Neonatal, Non-Familial .
Epilepsy, Benign Neonatal, Familial .
Epilepsy, Benign Neonatal, Non-Familial .
Epilepsy, Benign Neonatal, Nonfamilial .
Epilepsy, Benign Neonatal-Infantile .
Familial Benign Neonatal Convulsions .
Familial Benign Neonatal Epilepsy .
Non-Familial Benign Neonatal Convulsions .
Non-Familial Benign Neonatal Epilepsy .
Seizures, Benign Familial Infantile, 1 .
Seizures, Benign Familial Infantile, 3 .
Seizures, Benign Familial Neonatal-Infantile .
Benign Familial Neonatal Infantile Seizures .
Benign Neonatal Convulsion .
Benign Neonatal Epilepsies .
Benign Neonatal Non Familial Convulsions .
Benign Neonatal-Infantile Epilepsies .
Benign Neonatal-Infantile Epilepsy .
Benign Non Familial Neonatal Convulsions .
Convulsion, Benign Neonatal .
Convulsions, Benign Neonatal .
Epilepsies, Benign Neonatal .
Epilepsies, Benign Neonatal-Infantile .
Epilepsy, Benign Neonatal Infantile .
Neonatal Convulsion, Benign .
Neonatal Epilepsies, Benign .
Neonatal Epilepsy, Benign .
Neonatal-Infantile Epilepsies, Benign .
Neonatal-Infantile Epilepsy, Benign .
Non Familial Benign Neonatal Convulsions .
Non Familial Benign Neonatal Epilepsy .
Seizures, Benign Familial Neonatal Infantile .
Neonatal Convulsions, Benign .
A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11(2):51-5) .
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