Speech‐language performance and comorbid disorders in children with perisylvian syndrome induced by viral encephalitis

Autor: Dianrong Sun, Jianhui Zhao, Leihong Zhang, Rong Yu, Mei Hou

Publikováno v: Pediatric Investigation, Vol 8, Iss 3, Pp 177-183 (2024)

ABSTRACT Importance Viral encephalitis is one of the main causes of the perisylvian syndrome, which can cause damage to children's language‐speech, feeding, and swallowing functions. Comprehensive assessment of language‐speech and swallowing func

Externí odkaz: https://doaj.org/article/c4062238c72c46a397367e43a9b714b0

Congenital Perisylvian Syndrome: Magnetic Resonance Imaging Findings in Six Cases

Autor: Sugandhi Malgotra, Manik Mahajan, Smarth Nathyal, Savia Gupta, Vikrant Gupta

Publikováno v: JK Science, Vol 26, Iss 2 (2024)

Background: Congenital perisylvian syndrome is an extremely rare congenital neurological disorder associated with distinctive imaging findings. Herein we describe the clinical features and imaging appearance of congenital perisylvian syndrome on Magn

Externí odkaz: https://doaj.org/article/3d359ae17ab84f639df3e60c39858f08

Bilateral perisylvian syndrome management and drug-related problems

Autor: Nirupama Kulkarni, Sarwamangala S Nanjayyanamath, D S Usha, Sanatkumar B Nyamagoud

Publikováno v: Indian Journal of Health Sciences and Biomedical Research KLEU, Vol 16, Iss 1, Pp 163-165 (2023)

Perisylvian syndrome is a noncurable condition characterized by polymicrogyria in the perisylvian or perirolandic region. Perisylvian means the region or area of the brain that is responsible for language. The bilateral perisylvian syndrome is a cong

Externí odkaz: https://doaj.org/article/885dc7fc1304403a9cb8517f168a2847

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Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome

Autor: Bonardi, Claudia M., Bayat, Allan, Madsen, Camilla G⊘bel, Hammer, Trine B., Reale, Chiara, Gardella, Elena, Marjanovic, Dragan, Beniczky, Sandor, M⊘ller, Rikke S., Rubboli, Guido

Publikováno v: Bonardi, C M, Bayat, A, Madsen, C G, Hammer, T B, Reale, C, Gardella, E, Marjanovic, D, Beniczky, S, M⊘ller, R S & Rubboli, G 2022, ' Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome ', Epileptic Disorders, vol. 24, no. 3, pp. 577-582 . https://doi.org/10.1684/epd.2022.1423

We report the association, not previously described, between trisomy 20/ monosomy 18 and congenital bilateral perisylvian syndrome (CBPS), a condition featuring intellectual disability, epilepsy, oro-motor dysfunction and bilateral perisylvian polymi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61f74188c7c6e529a2bcc8f360626639
https://pure.au.dk/portal/da/publications/trisomy-20pmonosomy-18p-associated-with-congenital-bilateral-perisylvian-syndrome(d2eab872-e220-45c0-9523-dba96b17f8e7).html