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1.
Neurosciences (Riyadh) ; 10(1): 61-3, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22473187

RESUMO

OBJECTIVE: To explore the profile of cytosine/adenine/guanine (CAG) repeat expansion in Omani spinocerebellar ataxia (SCA) patients. METHODS: Ten SCA patients attending the Sultan Qaboos University Hospital Neurologic clinics, Al-Khoud, Oman in the 3 years starting from January 2000 were recruited for this study. Genomic DNA was extracted from peripheral blood samples and CAG repeat expansion analysis was carried out by polymerase chain reaction and sequencing, when required. RESULTS: The CAG triplet repeats leading to polyglutamine expansion and neurodegeneration are seen in spinocerebellar ataxias 1, 2, 3, 6, 7 and 17. By using primers for SCA 1, 2, 3 and 7, we found the repeats were in the normal range and triplet repeats do not seem to be a common cause for ataxia in Oman. CONCLUSION: Spinocerebellar ataxia in Oman has the normal range of CAG repeats for the commonly found SCA1, SCA2, SCA3 and SCA7.

3.
Acta Neurol Scand ; 91(2): 133-6, 1995 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-7785423

RESUMO

Olivopontocerebellar atrophy (OPCA) is rare in childhood and onset in infancy is uncommon. We encountered 11 consecutive children with clinical and radiological features of OPCA which started in infancy. In addition to cerebellar ataxia, these children also had sensorineural deafness and speech impairment. Of the present cases, 8 were sporadic and the pedigree patterns in 3 (with a sibling also involved) point to an AR inheritance. The CT scan showed varying degrees of cerebellar and pontine atrophy. The underlying genetic and neurochemical substrates of this syndrome await further study.


Assuntos
Surdez/genética , Atrofias Olivopontocerebelares/genética , Tronco Encefálico/patologia , Cerebelo/patologia , Ventrículos Cerebrais/patologia , Criança , Pré-Escolar , Cisterna Magna/patologia , Surdez/diagnóstico por imagem , Feminino , Humanos , Transtornos do Desenvolvimento da Linguagem/diagnóstico por imagem , Transtornos do Desenvolvimento da Linguagem/genética , Masculino , Exame Neurológico , Atrofias Olivopontocerebelares/diagnóstico por imagem , Fenótipo , Tomografia Computadorizada por Raios X
5.
Acta Neurol Scand ; 78(3): 185-9, 1988 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-3227804

RESUMO

Cognitive impairment has been reported to occur in minor head injury (concussion). The value of the P300 evoked potential as a measure of cerebral concussion was studied in 20 patients with minor head injury and compared with the data from 20 normal subjects. Significant abnormalities of the P300 latency and amplitude were noted in these patients in the post-concussion period. The abnormalities improved completely on repeat testing. The correlation of the P300 to other parameters of head injury is discussed. The P300 constitutes a simple laboratory test that is sensitive measure of cerebral dysfunction in concussive head injuries.


Assuntos
Nível de Alerta/fisiologia , Concussão Encefálica/fisiopatologia , Transtornos Cognitivos/fisiopatologia , Eletroencefalografia , Transtornos Neurocognitivos/fisiopatologia , Adolescente , Adulto , Atenção/fisiologia , Potenciais Evocados Auditivos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Discriminação da Altura Tonal/fisiologia , Tempo de Reação/fisiologia
6.
Aust N Z J Med ; 16(2): 234-5, 1986 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-3092792

RESUMO

A patient presented with elementary partial motor seizures on the same side as the cerebral lesion. A cerebral computerised tomographic scan showed a right medial frontal atrophic lesion and an electroencephalogram showed seizure discharges from the same region. The clinical significance and pathophysiology of ipsilateral seizures are discussed.


Assuntos
Epilepsias Parciais/diagnóstico por imagem , Adulto , Atrofia , Encéfalo/diagnóstico por imagem , Encéfalo/patologia , Eletroencefalografia , Epilepsias Parciais/patologia , Epilepsias Parciais/fisiopatologia , Humanos , Masculino , Tomografia Computadorizada por Raios X
8.
Clin Neurol Neurosurg ; 87(2): 113-7, 1985.
Artigo em Inglês | MEDLINE | ID: mdl-4028585

RESUMO

Bruxism, the phenomenon of non-functional grinding of the teeth has been ascribed to various causes. Twenty patients with coma from different causes who displayed bruxism were studied with an attempt to correlate the phenomenon to the level of consciousness, eye movements, respiration, cold caloric test, motor deficits and sleep wake cycles. Bruxism was seen to appear at different levels of consciousness, but to disappear only after a significant improvement in the level of consciousness. A relationship with the appearance of sleep wake cycles was also seen.


Assuntos
Bruxismo/etiologia , Coma/complicações , Adolescente , Adulto , Bruxismo/fisiopatologia , Testes Calóricos/métodos , Criança , Pré-Escolar , Temperatura Baixa , Coma/fisiopatologia , Estado de Consciência , Eletroencefalografia , Feminino , Humanos , Lactente , Masculino , Transtornos dos Movimentos/complicações , Respiração , Fases do Sono/fisiologia , Fatores de Tempo , Vigília/fisiologia
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