CLTM AND EEG BOARD COMBINED EXAM
2025/2026 BANK COMPLETE QUESTIONS
AND ANSWERS ACCURATE ACTUAL EXAM
WITH FREQUENTLY TESTED QUESTIONS
AND STUDY GUIDE / EXPERT VERIFIED
FOR GUARANTEED PASS/ALREADY
GRADED A+
What is the neuro-genetic disorder characterized by
intellectual and developmental delay, sleep disturbances,
seizures, jerky movements, frequent laughter or smiling,
and usually a happy demeanor? -
....ANSWER...Angelmans Syndrome
What is the first line agent for Lennox-Gastaut
Syndrome? - ....ANSWER...Valproic Acid (Valproate)
Which of the following seizure manifestations in Lennox
Gastaut would most likely be an indication for Corpus
Collusotomy?
,A. Drop Attacks/Atonic Seizure
B. Tonic Clonic Seizures
C. Automotisms - ....ANSWER...A. Drop Attacks/Atonic
Seizure
What is the surgical treatment for Lennox-Gastaut
Syndrome? - ....ANSWER...Multiple Subpial Transection
West Syndrome commonly evolves to: -
....ANSWER...Lennox-Gastaut Syndrome
What is the new term for Benign Rolandic Epilepsy? -
....ANSWER...Self Limited Epilepsy with Centrotemporal
Spikes
What electrodes are best to captured activity rom Self
Limited Epilepsy with Centrotemporal Spikes? -
....ANSWER...C1 and C2 of the international 10-10 system
of electrode placement are useful in a patient suspected of
having Benign Rolandic Epilepsy
,Treatment for Self Limited Epilepsy with Centrotemporal
Spikes (Benign Rolandic Epilepsy) -
....ANSWER...Neurontin (Gabapentin)
Trileptal (Oxcarbazepine)
Tegretol or Carbatrol (Carbamazepine)
Many not medicated secondary to frequency & nocturnal
occurrence
Onset 15 months - 15 years (usually 4-8 years)
Initial seizure manifestations include visual hallucinations
(flashing lights), blindness, amaurosis, micropsia,
metamorphopsia
Loss of consciousness can occur
Can have migraine and nausea afterward
EEG show occipital spikes and wave 1.5-2.5Hz
Eye opening enhances and sleep inhibits -
....ANSWER...Benign Occipital Epilepsy
What is the typical age range for the onset of Landau-
Kleffner Syndrome? - ....ANSWER...2-12 years
, What are some common symptoms of Landau-Kleffner
Syndrome related to language and speech? -
....ANSWER...Acquired aphasia, verbal auditory agnosia,
decreased spontaneous speech, dysphagia
What are some cognitive features associated with Landau-
Kleffner Syndrome? - ....ANSWER...Difficulty
understanding speech, neuropsychological disturbances in
>50%, normal intelligence
What types of seizures are commonly seen in Landau-
Kleffner Syndrome? - ....ANSWER...Generalized tonic-
clonic, Myoclonic, Absence
What EEG findings are characteristic of Landau-Kleffner
Syndrome? - ....ANSWER...Normal during wakefulness,
spike & wave during sleep (mostly in partial and temporal
lobes), electrical status epilepticus of sleep
What is the best activation procedure for Landau-Kleffner
syndrome? - ....ANSWER...Sleep
Various seizure types occur during sleep.
2025/2026 BANK COMPLETE QUESTIONS
AND ANSWERS ACCURATE ACTUAL EXAM
WITH FREQUENTLY TESTED QUESTIONS
AND STUDY GUIDE / EXPERT VERIFIED
FOR GUARANTEED PASS/ALREADY
GRADED A+
What is the neuro-genetic disorder characterized by
intellectual and developmental delay, sleep disturbances,
seizures, jerky movements, frequent laughter or smiling,
and usually a happy demeanor? -
....ANSWER...Angelmans Syndrome
What is the first line agent for Lennox-Gastaut
Syndrome? - ....ANSWER...Valproic Acid (Valproate)
Which of the following seizure manifestations in Lennox
Gastaut would most likely be an indication for Corpus
Collusotomy?
,A. Drop Attacks/Atonic Seizure
B. Tonic Clonic Seizures
C. Automotisms - ....ANSWER...A. Drop Attacks/Atonic
Seizure
What is the surgical treatment for Lennox-Gastaut
Syndrome? - ....ANSWER...Multiple Subpial Transection
West Syndrome commonly evolves to: -
....ANSWER...Lennox-Gastaut Syndrome
What is the new term for Benign Rolandic Epilepsy? -
....ANSWER...Self Limited Epilepsy with Centrotemporal
Spikes
What electrodes are best to captured activity rom Self
Limited Epilepsy with Centrotemporal Spikes? -
....ANSWER...C1 and C2 of the international 10-10 system
of electrode placement are useful in a patient suspected of
having Benign Rolandic Epilepsy
,Treatment for Self Limited Epilepsy with Centrotemporal
Spikes (Benign Rolandic Epilepsy) -
....ANSWER...Neurontin (Gabapentin)
Trileptal (Oxcarbazepine)
Tegretol or Carbatrol (Carbamazepine)
Many not medicated secondary to frequency & nocturnal
occurrence
Onset 15 months - 15 years (usually 4-8 years)
Initial seizure manifestations include visual hallucinations
(flashing lights), blindness, amaurosis, micropsia,
metamorphopsia
Loss of consciousness can occur
Can have migraine and nausea afterward
EEG show occipital spikes and wave 1.5-2.5Hz
Eye opening enhances and sleep inhibits -
....ANSWER...Benign Occipital Epilepsy
What is the typical age range for the onset of Landau-
Kleffner Syndrome? - ....ANSWER...2-12 years
, What are some common symptoms of Landau-Kleffner
Syndrome related to language and speech? -
....ANSWER...Acquired aphasia, verbal auditory agnosia,
decreased spontaneous speech, dysphagia
What are some cognitive features associated with Landau-
Kleffner Syndrome? - ....ANSWER...Difficulty
understanding speech, neuropsychological disturbances in
>50%, normal intelligence
What types of seizures are commonly seen in Landau-
Kleffner Syndrome? - ....ANSWER...Generalized tonic-
clonic, Myoclonic, Absence
What EEG findings are characteristic of Landau-Kleffner
Syndrome? - ....ANSWER...Normal during wakefulness,
spike & wave during sleep (mostly in partial and temporal
lobes), electrical status epilepticus of sleep
What is the best activation procedure for Landau-Kleffner
syndrome? - ....ANSWER...Sleep
Various seizure types occur during sleep.
