Myoclonic Epilepsies (Myoclonic Encephalopathy)
338
relevant articles (18 outcomes,
18 trials/studies)
found for this Disease
Description:
A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic (i.e., occurring secondary to known disease processes such as infections, hypoxic-ischemic injuries, trauma, etc.).
Also Known As:
Myoclonic Encephalopathy; Epilepsy, Myoclonus; Epilepsy, Myoclonic; Myoclonus Epilepsy; Myoclonic Epilepsy; Absence Epilepsy, Myoclonic; Epilepsies, Myoclonic; Benign Infantile Myoclonic Epilepsy; Cryptogenic Myoclonic Epilepsy; Early Childhood Epilepsy, Myoclonic; Early Childhood, Myoclonic Epilepsy; Encephalopathy, Myoclonic; Epilepsy, Early Childhood, Myoclonic; Epilepsy, Myoclonic, Early Childhood; Epilepsy, Myoclonic, Infantile; Epilepsy, Myoclonic, Infantile, Benign; Epilepsy, Myoclonic, Infantile, Severe; Infantile Severe Myoclonic Epilepsy; Myoclonic Astatic Epilepsy; Myoclonic Epilepsy, Benign Infantile; Myoclonic Epilepsy, Early Childhood; Myoclonic Epilepsy, Infantile, Benign; Myoclonic Epilepsy, Infantile, Severe; Myoclonic Epilepsy, Severe Infantile; Myoclonic Seizure Disorder; Severe Infantile Myoclonic Epilepsy; Severe Myoclonic Epilepsy, Infantile; Absence Epilepsies, Myoclonic; Astatic Epilepsies, Myoclonic; Astatic Epilepsy, Myoclonic; Cryptogenic Myoclonic Epilepsies; Disorder, Myoclonic Seizure; Disorders, Myoclonic Seizure; Encephalopathies, Myoclonic; Epilepsies, Cryptogenic Myoclonic; Epilepsies, Idiopathic Myoclonic; Epilepsies, Myoclonic Absence; Epilepsies, Myoclonic Astatic; Epilepsies, Symptomatic Myoclonic; Epilepsy, Cryptogenic Myoclonic; Epilepsy, Idiopathic Myoclonic; Epilepsy, Myoclonic Absence; Epilepsy, Myoclonic Astatic; Epilepsy, Symptomatic Myoclonic; Idiopathic Myoclonic Epilepsies; Myoclonic Absence Epilepsies; Myoclonic Astatic Epilepsies; Myoclonic Encephalopathies; Myoclonic Epilepsies, Cryptogenic; Myoclonic Epilepsies, Idiopathic; Myoclonic Epilepsies, Symptomatic; Myoclonic Epilepsy, Cryptogenic; Myoclonic Epilepsy, Idiopathic; Myoclonic Seizure Disorders; Myoclonus Epilepsies; Seizure Disorder, Myoclonic; Seizure Disorders, Myoclonic; Symptomatic Myoclonic Epilepsies; Idiopathic Myoclonic Epilepsy; Myoclonic Absence Epilepsy; Symptomatic Myoclonic Epilepsy
Relationship Network
Disease Context: Research Results
Related Diseases
Experts
| 1. | Yu, Frank H:
3 articles
(12/2007 - 09/2006)
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| 2. | Catterall, William A:
3 articles
(12/2007 - 09/2006)
|
| 3. | Westenbroek, Ruth E:
2 articles
(10/2007 - 09/2006)
|
| 4. | Kalume, Franck:
2 articles
(10/2007 - 09/2006)
|
| 5. | Scheuer, Todd:
2 articles
(10/2007 - 09/2006)
|
| 6. | Veggiotti, Pierangelo:
2 articles
(01/2006 - 03/2002)
|
| 7. | Osawa, M:
2 articles
(01/2005 - 10/2001)
|
| 8. | Yamamoto, T:
2 articles
(09/2003 - 03/2001)
|
| 9. | Tommerup, Niels:
1 article
(06/2008)
|
| 10. | Schneider, Lizette M:
1 article
(06/2008)
|
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Myoclonic Epilepsies:
| 1. | Valproic Acid (Valproate, Semisodium)FDA LinkGeneric
10/01/2002
- " She was diagnosed as having benign myoclonic epilepsy of infancy at 3.5 months of age and treated with valproic acid" 07/01/1987
- " A mentally retarded 23-year-old woman with myoclonic astatic epilepsy developed an abnormal posture of extreme forward flexion, called camptocormia, during valproate monotherapy" 09/01/2008
- " In 5 pediatric patients with severe myoclonic epilepsy and valproic acid-induced liver failure, we identified 1 novel and 4 previously described pathogenic mutations in the linker region of this enzyme" 02/01/1977
- " Sodium valproate alone controlled all fits in four children with absences, in 18 with absences with automatisms, 10 with tonic-clonic seizures and 22 with myoclonic epilepsy" 11/10/1978
- " Valproic acid, a new anticonvulsant, is most effective in absence seizures (simple and complex), but it has produced improvement in tonicclonic seizures, mixed absence with tonic-clonic seizures, and myoclonic epilepsy"
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| 2. | clobazam (HR 376)IBA
11/01/1999
- " Ten of the 20 children with severe myoclonic epilepsy in infancy also responded with clobazam (CLB) as comedication" 01/01/2007
- " Whereas the studies in adult patients were disappointing, the trials conducted in pediatric populations demonstrated a specific efficacy of STP in severe myoclonic epilepsy in infancy, Dravet syndrome, when combined with valproate and clobazam" 07/01/2005
- " Although the studies in adult patients were disappointing, the trials conducted in paediatric populations demonstrated a specific efficacy of STP in a severe form of early childhood epilepsy, Dravet syndrome (severe myoclonic epilepsy in infancy), when combined with valproate and clobazam" 04/01/2006
- " A metabolic interaction between stiripentol (STP), an anticonvulsant agent that inhibits the activity of several cytochromes P450 (P450s), and clobazam (CLB), a 1,5-benzodiazepine, used in association with STP in severe myoclonic epilepsy in infancy was observed in vivo" 04/01/2005
- " 6) The stiripentol dose strengths currently available in France are unsuitable for infants weighing less than 10 kg. (7) In practice, given the severity of this type of myoclonic epilepsy of infancy, the addition of stiripentol to ongoing but ineffective valproate-clobazam combination therapy is justified, even though the treatment is somewhat difficult to manage and has not yet been fully evaluated."
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| 3. | stiripentolIBA
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| 4. | BismuthIBA
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| 5. | Anticonvulsants (Antiepileptic Drugs)IBA
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| 6. | etiracetam (levetiracetam)FDA Link
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| 7. | SaltsIBA
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| 8. | lamotrigine (Lamictal)FDA LinkGeneric
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| 9. | VigabatrinIBA
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| 10. | Clonazepam (Rivotril)FDA LinkGeneric
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Therapies and Procedures