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1. Introduction
2. Incidence of unprovoked seizures
3. Classification of epileptic seizures
4. Prevalence of generalized and partial seizures
5. Complex partial seizure in child
6. Complex partial seizure - EEG
7. Complex partial seizure - MRI scan
8. Inter-ictal and ictal SPECT scans
9. Simple partial seizure in child
10. Partial seizure with secondary generalization
11. Generalized tonic-clonic seizure in child
12. Epileptic syndrome
13. Describing a seizure (Dr. Dreifuss)
14. Importance of diagnosing epileptic syndromes
15. Tonic seizures in newborn
16. Benign familial neonatal seizures
17. K+ currents in BFNC
18. Severe myoclonic epilepsy of infancy
19. Generalized epilepsy with febrile seizures+
20. GEFS+ - aberrant Na+ channel
21. Locus heterogeneity and variable expressivity
22. Idiopathic focal epilepsies of infancy and childhood
23. Occipital spikes - EEG
24. Benign Rolandic epilepsy
25. Benign Rolandic epilepsy-clinical phenomenon
26. Benign Rolandic epilepsy-EEG
27. Midtemporal central spikes - EEG
28. Rolandic spikes - EEG
29. Rolandic and occipital spikes - EEG
30. Idiopathic generalized epilepsies
31. Absence seizure in child
32. Absence seizure - EEG
33. Generalized tonic clonic seizure in child
34. Generalized tonic clonic seizure - EEG
35. Generalized spiking wave on EEG
36. Epileptic encephalopathies
37. Infantile spasms
38. Hypsarrhythmia on EEG
39. Infantile spasm in child
40. Lennox-Gastaut syndrome
41. Lennox-Gastaut syndrome - atypical absence
42. Lennox-Gastaut syndrome - tonic seizure
43. Tonic seizure in patient
44. Epilepsy and other neurological disturbances
45. Angelman syndrome (1)
46. Angelman syndrome (2)
47. Angelman syndrome - consistent findings
48. Angelman syndrome frequent findings
49. Angelman syndrome - seizures
50. Angelman syndrome - EEG (1)
51. Angelman syndrome - rhythmic slowing on EEG
52. Angelman syndrome-caused by genetic imprinting
53. Genetic mechanisms of AS and PWS
54. Angelman syndrome-GABA(A) subunit mutations
55. The GABA receptor
56. Angelman syndrome-mutations in ubiquitin ligase
57. Angelman syndrome-phenotype and genotype
58. Tuberous sclerosis
59. Tuberous sclerosis - MRI
60. Tuberous sclerosis - genetic associations
61. TSC1/TSC2 pathway
62. Tuberous sclerosis (2)
63. Special issues in patients with tuberous sclerosis
64. Seizure remission and AED discontinuation in TSC
65. Rett syndrome
66. Rett syndrome - genetic causes
67. Fragile X
68. Lissencephaly (1)
69. Lissencephaly (2)
70. Lissencephaly (3)
71. Conclusions
72. Thank you

Topics Covered

• Incidence of Seizures
• Classification of Seizures
• Prevalence of Generalized and Partial Seizures
• Epileptic Syndromes
• Benign Familial Neonatal Seizures
• Generalized Epilepsy Febrile Seizures +
• Idiopathic Focal Epilepsies of Infancy and Childhood
• Benign Rolandic Epilepsy
• Idiopathic Generalized Seizures
• Epileptic Encephalopathies
• Infantile Spasms
• Lennox-Gastaut Syndrome
• Epilepsy in Association with Other Neurological Conditions
• Angelman Syndrome
• Tuberous Sclerosis
• Rett Syndrome
• Fragile X Syndrome
• Lissencephaly

Links

Series:

• Epilepsy and Seizures

Categories:

• Clinical Practice
• Neuroscience

Therapeutic Areas:

• Neurology

Talk Citation

Publication History

• Published on May 4, 2011
• Archived on May 30, 2021

Financial Disclosures

• Dr. Gregory L. Holmes has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.