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1.
Acta Paediatr ; 93(4): 523-8, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15188981

RESUMO

AIM: To evaluate the role of early (up to 12 h) changes in cerebral blood-flow (CBF) velocity in predicting the severity of hypoxic-ischaemic encephalopathy (HIE) and long-term outcome in asphyxiated term infants. METHODS: CBF velocities were investigated by colour Doppler ultrasonography in 81 healthy and 60 asphyxiated term infants at least three times during the first 5 d of life. The psychomotor development of infants was followed up to 18 mo. RESULTS: No differences in CBF velocities were found at the age of 2-6 h between infants with severe and mild-moderate HIE, mean CBF velocity [mean (95% CI of mean CBF velocity)] in anterior cerebral artery [14.9 (1.4-28.4)cm/s] and [13.9 (11.1-16.7) cm/s], respectively, and between infants with poor outcome (death or severe disability) and with normal development/mild impairments. By the age of 12 h infants with mild-moderate HIE and infants with normal development/mild impairments had decreased CBF velocity in the anterior cerebral artery, and infants with severe HIE or poor outcome had increased mean CBF velocity in anterior, medial cerebral and basilar artery compared to the control group. CONCLUSION: The value of CBF velocity changes to predict poor outcome in asphyxiated infants is low 2-6 h after asphyxia, but increases by the age of 12 ho.


Assuntos
Asfixia Neonatal/fisiopatologia , Artérias Cerebrais/fisiopatologia , Circulação Cerebrovascular , Índice de Apgar , Asfixia Neonatal/diagnóstico por imagem , Velocidade do Fluxo Sanguíneo , Estudos de Casos e Controles , Artérias Cerebrais/diagnóstico por imagem , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Masculino , Avaliação de Resultados em Cuidados de Saúde , Valor Preditivo dos Testes , Prognóstico , Estudos Prospectivos , Valores de Referência , Sensibilidade e Especificidade , Ultrassonografia Doppler em Cores
2.
Brain Dev ; 23(4): 236-9, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11377002

RESUMO

We reported four cases of Hallervorden-Spatz disease. All four siblings (three males and one female) in the family are affected. The first symptoms of the disease were spastic paraparesis and optic atrophy followed by trunkal dystonia and lower motor neurone involvement. The average age of the onset was 4.25 years. The diagnosis was made at the ages of 17, 14, 11 and 10 years. The diagnosis was confirmed clinically, electrophysiologically and by MRI. On MRI scans all patients demonstrated hypointense areas in globus pallidus. There is neither specific treatment nor prenatal diagnosis.


Assuntos
Espasticidade Muscular/diagnóstico , Atrofias Ópticas Hereditárias/diagnóstico , Neurodegeneração Associada a Pantotenato-Quinase/diagnóstico , Adolescente , Adulto , Criança , Feminino , Humanos , Masculino , Espasticidade Muscular/etiologia , Espasticidade Muscular/genética , Núcleo Familiar , Atrofias Ópticas Hereditárias/etiologia , Atrofias Ópticas Hereditárias/genética , Neurodegeneração Associada a Pantotenato-Quinase/complicações , Neurodegeneração Associada a Pantotenato-Quinase/genética
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