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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 .
C10.228.140.490.375 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 .
C10.597.742.785 Status Epilepticus .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.742 Seizures .
C23.888.592.742.785 Status Epilepticus .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
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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563336
 
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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21546
 
Epilepsy .
Epilepsy, Cryptogenic .
Auras .
Cryptogenic Epilepsies .
Cryptogenic Epilepsy .
Epilepsies .
Epilepsies, Cryptogenic .
Epilepsy, Awakening .
Seizure Disorders .
Aura 3776 .
Awakening Epilepsy .
Seizure Disorder .
Epileptic Seizures .
A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) .
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213360814
 
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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Status Epilepticus .
Grand Mal Status Epilepticus .
Status Epilepticus, Complex Partial .
Status Epilepticus, Electrographic .
Status Epilepticus, Generalized .
Status Epilepticus, Generalized Convulsive .
Status Epilepticus, Grand Mal .
Status Epilepticus, Non-Convulsive .
Status Epilepticus, Simple Partial .
Status Epilepticus, Subclinical .
Electrographic Status Epilepticus .
Generalized Status Epilepticus .
Non Convulsive Status Epilepticus .
Status Epilepticus, Non Convulsive .
Status, Absence .
Status, Petit Mal .
Subclinical Status Epilepticus .
Petit Mal Status .
Absence Status .
Complex Partial Status Epilepticus .
Generalized Convulsive Status Epilepticus .
Non-Convulsive Status Epilepticus .
Simple Partial Status Epilepticus .
A prolonged seizure or seizures repeated frequently enough to prevent recovery between episodes occurring over a period of 20-30 minutes. The most common subtype is generalized tonic-clonic status epilepticus, a potentially fatal condition associated with neuronal injury and respiratory and metabolic dysfunction. Nonconvulsive forms include petit mal status and complex partial status, which may manifest as behavioral disturbances. Simple partial status epilepticus consists of persistent motor, sensory, or autonomic seizures that do not impair cognition (see also EPILEPSIA PARTIALIS CONTINUA). Subclinical status epilepticus generally refers to seizures occurring in an unresponsive or comatose individual in the absence of overt signs of seizure activity. (From N Engl J Med 1998 Apr 2;338(14):970-6; Neurologia 1997 Dec;12 Suppl 6:25-30) .
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