serw-MX  [xml]  
 


    
 DeCS Categories

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.708 Osteochondrodysplasias .
C05.116.099.708.779 Pycnodysostosis .
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 .
C10.228.140.490.375 Epilepsy, Generalized .
C10.228.140.490.375.260 Epilepsy, Absence .
C10.228.140.490.493 Epileptic Syndromes .
C10.228.140.490.493.125 Epilepsy, Absence .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.800 Pycnodysostosis .
C16.320.812 Pycnodysostosis .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.800 Pycnodysostosis .
D02 Organic Chemicals .
D02.478 Imides .
D02.478.770 Succinimides .
D02.478.770.333 Ethosuximide .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.773 Pyrrolidines .
D03.383.773.812 Pyrrolidinones .
D03.383.773.812.852 Succinimides .
D03.383.773.812.852.333 Ethosuximide .
 
 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) .
1.00
563336
 
Ethosuximide .
Emeside .
Ethylmethylsuccimide .
Ethymal .
Etosuximida Faes .
Petnidan .
Pyknolepsinum .
Suksilep .
Suxilep .
Zarontin .
Faes, Etosuximida .
Ethosuccimid .
An anticonvulsant especially useful in the treatment of absence seizures unaccompanied by other types of seizures. .
0.66
11854
 
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) .
0.66
213160814
 
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) .
0.56
1548102
 
Pycnodysostosis .
Pycnodysostoses .
Pyknodysostoses .
Pyknodysostosis .
Rare autosomal recessive syndrome characterized by delayed closing of CRANIAL SUTURES, short stature, ACRO-OSTEOLYSIS of distal phalanges, dental and MAXILLOFACIAL ABNORMALITIES and an increase in bone density that results in frequent BONE FRACTURES. It is associated with BONE RESORPTION defect due to mutations in the lysosomal cysteine protease CATHEPSIN K. .
0.53
454