Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Worster Drought syndrome"'
Autor:
Marcio Gadelha Vasconcelos, José Antonio Fiorot Jr, Caroline Sarkovas, Aline Pereira Martins Pinto, Orlando G P Barsottini, Alberto Alain Gabbai
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 64, Iss 2a, Pp 322-325 (2006)
A síndrome de Foix-Chavany-Marie (SFCM) caracteriza-se por apraxia da fala associada à paralisia bilateral da face, palato mole, língua e musculatura da faringe, mas com preservação das funções reflexas e automáticas. Na síndrome de Worster-
Externí odkaz:
https://doaj.org/article/3ac16bbdf52744f0a25458d7c11d04bf
Autor:
Fernanda Queirós, Gleison Duarte, Cecília Correia, Juliana Gomes Sérgio, Camila Vila-Nova, Rita Lucena
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 62, Iss 3b, Pp 906-910 (2004)
A síndrome de Worster-Drought é entidade clínica decorrente de lesão do trato cortico-nuclear. Não existe etiologia definida e caracteriza-se por alteração do controle voluntário e involuntário dos músculos que movimentam lábios, mandíbul
Externí odkaz:
https://doaj.org/article/0d09913a1921439690ba3dfaae0827b5
Akademický článek
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Publikováno v:
Child Neurology Open
Child Neurology Open, Vol 5 (2018)
Child Neurology Open, Vol 5 (2018)
Worster-Drought syndrome is a congenital, pseudobulbar paresis. There is no identified molecular etiology despite familial cases reported. The authors report a boy who was diagnosed with Worster-Drought syndrome due to longstanding drooling, dysphagi
Autor:
Masayuki Sasaki, Eiji Nakagawa, Masato Hiyane, Noriko Sato, Yoko Imai, Hirofumi Komaki, Toshiyuki Yamamoto, Kenji Sugai, Takashi Saito, Yoshiaki Saito
Publikováno v:
Brain and Development. 34:787-791
In this study, we present the case of a 2-year-old boy who exhibited facial and bulbar paralysis since birth, severe dysphagia, signs of oculomotor disturbance, jaw jerks, pyramidal signs on both toes, intellectual disability, and severe gastroesopha
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45:S50-S50
Background: Worster-Drought syndrome (WDS) is a congenital, pseudobulbar paresis. Patients show oromotor apraxia causing impaired speech, drooling, dysphagia and varying degrees of cognitive impairment. Familial cases are reported although causative
Publikováno v:
Developmental Medicine & Child Neurology. 52:27-32
AIM Worster-Drought syndrome (WDS), or congenital suprabulbar paresis, is a permanent movement disorder of the bulbar muscles causing persistent difficulties with swallowing, feeding, speech, and saliva control owing to a non-progressive disturbance
Autor:
Jayakumar Paramasivam, Praveen Kumar Jayakumar, Gayathri Praveen Kumar, Alex Mathews Muruppel, Naveen Kumar Jayakumar
Background and aims: An out-patient surgical procedure in the paediatric age group is a tough task for a surgeon, more so when compounded with mentally challenging conditions like cerebral palsy. Every step involved, either administration of local an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c35e665d6b22c86bbb9773f17f550d2
https://europepmc.org/articles/PMC4523597/
https://europepmc.org/articles/PMC4523597/
Publikováno v:
Developmental Medicine & Child Neurology. 42:122-132
Foix-Chavany-Marie syndrome (FCMS) is a distinct clinical picture of suprabulbar (pseudobulbar) palsy due to bilateral anterior opercular lesions. Symptoms include anarthria/severe dysarthria and loss of voluntary muscular functions of the face and t
Autor:
S. Purkayastha
Publikováno v:
The Neuroradiology Journal. 21:306-308
Worster-Drought syndrome (WDS) (congenital bilateral perisylvian syndrome, congenital pseudobulbar paresia) is characterized by neuronal migration defect, pseudobulbar paralysis, epilepsy, neuromotor retardation and perisylvian dysplasia. Pituitary a