Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtre
Ajouter des filtres








Gamme d'année
1.
Arq. neuropsiquiatr ; 61(4): 909-915, Dec. 2003. tab
Article Dans Anglais | LILACS | ID: lil-352424

Résumé

Rett syndrome (RS) is a neurodevelopmental disorder, preferentially found in females and specifically involving the functions on which intelligence and its expression depend - learning, hand use and speech - leaving many others intact. Mutations have been identified at Xq28 on the MECP2 gene (methyl-CpG 2), which selectively silences the expression of other genes whose location is still unknown. This is a study on clinical, diagnostic and epidemiological aspects of RS in a Brazilian sample. It included 33 female patients with chronic encephalopathy without known etiology. RS was diagnosed in 24 patients (72.7 percent): 17 (70.8 percent) had classical RS; 5 (20.8 percent), atypical RS and 2 (8.4 percent), potential RS. In 9 girls clinical data and/or laboratory studies excluded diagnosis of RS. Among the atypical RS patients, 4 were form fruste and one, congenital form. Among the girls with other encephalopathies, cerebral malformation was the most frequent finding


Sujets)
Humains , Femelle , Enfant d'âge préscolaire , Enfant , Adolescent , Souffrance cérébrale chronique/physiopathologie , Syndrome de Rett/diagnostic , Répartition par âge , Âge de début , Brésil/épidémiologie , Ilots CpG , Protéines de liaison à l'ADN/génétique , Électroencéphalographie , Études de suivi , Génotype , Mutation , Phénotype , Prévalence , Syndrome de Rett/épidémiologie , Syndrome de Rett/génétique
2.
Arq. neuropsiquiatr ; 61(3B): 859-863, Sept. 2003. ilus
Article Dans Portugais | LILACS | ID: lil-348668

Résumé

Apresentamos dois casos de histoplasmose em que o acometimento do sistema nervoso central foi a única manifestaçäo clínica da doença. Revisäo da literatura permitiu confirmar a raridade dessa forma de patologia, em particular em crianças, sendo o segundo caso aqui apresentado o de mais baixa idade na literatura nacional. Säo feitos comentários sobre a variedade das apresentaçöes clínicas e os principais diagnósticos diferenciais da doença. Säo discutidos os resultados laboratoriais, tanto em relaçäo às alteraçöes liquóricas quanto aos resultados sorológicos. Finalmente, é analisada a terapêutica dessa forma de infecçäo fúngica tanto em relaçäo aos medicamentos utilizáveis quanto à duraçäo prolongada aconselhável para o tratamento específico


Sujets)
Humains , Mâle , Femelle , Enfant , Adulte , Infections fongiques du système nerveux central , Histoplasmose , Antifongiques , Infections fongiques du système nerveux central , Fluconazole , Histoplasmose , Imagerie par résonance magnétique
SÉLECTION CITATIONS
Détails de la recherche