合計: 16 |
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PMID (PMCID) | ||
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24950661 |
MALE | Infant |
A case of startle epilepsy associated with IL1RAPL1 gene deletion. | ||
Dinopoulos A, Stefanou MI, Attilakos A, Tsirouda M, Papaevangelou V. Pediatr Neurol. 2014;51(2):271-4. |
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Startle epilepsy is a type of reflex epilepsy in which the seizures are mainly precipitated by unexpected sensory stimuli. | ||
23531553 |
FEMALE | |
Corpus callosotomy in a patient with startle epilepsy. | ||
Gomez NG, Hamad AP, Marinho M, Tavares IM, Carrete H Jr, Caboclo LO Jr, Yacubian EM Jr, Centeno R Jr. Epileptic Disord. 2013;15(1):76-9. |
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Corpus callosotomy may be considered in patients with startle epilepsy and tonic seizures, in the absence of focal lesions amenable to surgery. | ||
23531553 |
FEMALE | |
Corpus callosotomy in a patient with startle epilepsy. | ||
Gomez NG, Hamad AP, Marinho M, Tavares IM, Carrete H Jr, Caboclo LO Jr, Yacubian EM Jr, Centeno R Jr. Epileptic Disord. 2013;15(1):76-9. |
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Startle epilepsy is a syndrome of reflex epilepsy in which the seizures are precipitated by a sudden and surprising, usually auditory, stimulus. | ||
23141145 |
MALE | |
Seizure-free after surgery in a patient with non-lesional startle epilepsy: a case report. | ||
Sun YP, Zhu HW, Zhang SW, Huang ZY, Li LP, Qiao L, Du W, Wang YP. Epilepsy Behav. 2012;25(4):700-3. |
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Seizure-free after surgery in a patient with non-lesional startle epilepsy: a case report. | ||
22675038 |
MALE | Middle Aged |
Adult onset startle epilepsy. | ||
Moseley BD, Shin C. BMJ Case Rep. 2011;2011:. |
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The present case demonstrates that startle epilepsy can rarely be diagnosed in adults; typically seizure onset in this condition is during infancy to childhood. | ||
19400869 |
FEMALE | Child |
Startle epilepsy associated with gait-induced seizures: Pathomechanism analysis using EEG, MEG, and PET studies. | ||
Saeki K, Saito Y, Sugai K, Nakagawa E, Komaki H, Sakuma H, Sasaki M, Kaneko Y. Epilepsia. 2009;50(5):1274-9. |
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Startle epilepsy associated with gait-induced seizures: Pathomechanism analysis using EEG, MEG, and PET studies. | ||
15668049 |
MIXED_SAMPLE | Child |
The movement disorders of Coffin-Lowry syndrome. | ||
Stephenson JB, Hoffman MC, Russell AJ, Falconer J, Beach RC, Tolmie JL, McWilliam RC, Zuberi SM. Brain Dev. 2005;27(2):108-13. |
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One of our adult patients had several types of movement disorder and epilepsy that merged seamlessly: there was true cataplexy triggered by telling a joke, something close to cataplexy ('cataplexy') triggered by sound-startle, a predominantly hypertonic reaction varying from hyperekplexia to a more prolonged tonic reaction resembling startle epilepsy, and true unprovoked epileptic seizures. | ||
15324827 |
MALE | Child |
Intractable reflex audiogenic epilepsy successfully treated by peri-insular hemispherotomy. | ||
Martinez-Manas R, Daniel RT, Debatisse D, Maeder-Ingvar M, Meagher-Villemure K, Villemure JG, Deonna T. Seizure. 2004;13(7):486-90. |
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We report a case of an infantile hemiplegia seizure syndrome (IHSS) that presented with intractable reflex audiogenic startle epilepsy which in itself is an uncommon form of seizure disorder. | ||
15324827 |
MALE | Child |
Intractable reflex audiogenic epilepsy successfully treated by peri-insular hemispherotomy. | ||
Martinez-Manas R, Daniel RT, Debatisse D, Maeder-Ingvar M, Meagher-Villemure K, Villemure JG, Deonna T. Seizure. 2004;13(7):486-90. |
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We report a case of an infantile hemiplegia seizure syndrome (IHSS) that presented with intractable reflex audiogenic startle epilepsy which in itself is an uncommon form of seizure disorder. | ||
10746422 |
MALE | Child |
Postoperative seizure outcome after corpus callosotomy in reflex epilepsy. | ||
Kwan SY, Wong TT, Chang KP, Yang TF, Lee YC, Guo WY, Su MS. Zhonghua Yi Xue Za Zhi (Taipei). 2000;63(3):240-6. |
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Patient 1 had Lennox-Gastaut syndrome with auditory-induced generalized atonic or tonic seizures (startle epilepsy), which decreased by 60% after callosotomy. | ||
10403230 |
FEMALE | Adult |
A case of startle epilepsy and SSMA seizures documented with subdural recordings. | ||
Serles W, Leutmezer F, Pataraia E, Olbrich A, Groppel G, Czech T, Baumgartner C. Epilepsia. 1999;40(7):1031-5. |
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A case of startle epilepsy and SSMA seizures documented with subdural recordings. | ||
9578019 |
MALE | Adult |
Startle epilepsy with infantile hemiplegia: report of two cases improved by surgery. | ||
Oguni H, Hayashi K, Usui N, Osawa M, Shimizu H. Epilepsia. 1998;39(1):93-8. |
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To study the effectiveness of surgical therapy on 2 patients with startle epilepsy with infantile brain damage (SEIBD), a rare but distinctive epileptic syndrome characterized by motor seizures resistant to antiepileptic drugs (AEDs). | ||
8805177 |
MALE | |
Vomiting attack with ACTH and ADH discharge improves startle epilepsy. | ||
Hayashi M, Yasaka A, Maruki K. Pediatr Neurol. 1996;14(4):322-5. |
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Because startle-induced epileptic seizures are resistant to conventional antiepileptic therapy, this case is informative for the treatment of startle epilepsy. | ||
6444792 |
FEMALE | Adult |
Startle epilepsy complicating Down syndrome during adulthood. | ||
Gimenez-Roldan S, Martin M. Ann Neurol. 1980;7(1):78-80. |
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A woman with Down syndrome--a trisomy 21 karyotype--developed severe startle epilepsy and spontaneous seizures at the age of 20 years. | ||
6444792 |
FEMALE | Adult |
Startle epilepsy complicating Down syndrome during adulthood. | ||
Gimenez-Roldan S, Martin M. Ann Neurol. 1980;7(1):78-80. |
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Triggering factors, seizure patterns, and ictal electroencephalograms were the same as in startle epilepsy occurring in children with cerebral palsy but differed in that there was no clinical or radiological evidence of a focal brain lesion in the vicinity of the motor supplementary cortex. | ||
6894024 |
FEMALE | Child |
The "startle disease" in brain-damaged patients: report of a case. | ||
Baier WK. Neuropadiatrie. 1980;11(1):72-5. |
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Furthermore, two related, non-epileptic paroxysmal startle syndromes, the "essential startle disease" and the "hereditary startle syndrome" are described and contrasted with "epileptic seizures induced by unexpected sensory stimuli" or "startle epilepsy". |