Meningomyelocele
Mostrando 1-10 de 10 artigos, teses e dissertações.
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1. Validade e confiabilidade de \"Questionário de qualidade de vida de pessoas com Espinha Bífida / Validity and reliability of the Questionário de Qualidade de Vida para Pessoas com Espinha Bífida
Objetivo: verificar a validade e a confiabilidade do Questionário de Qualidade de Vida para Pessoas com Espinha Bífida na língua Portuguesa, após tradução e adaptação cultural do Spina Bífida Health Related Quality of Life Questionnaire (HRQOL). Métodos: Dois professores de inglês realizaram a tradução literária e conceitual das versões para c
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 15/12/2011
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2. Desafios à inclusão de pessoas com deficiência: aspectos da trajetória escolar de crianças com lesão medular por mielomeningocele.
O objetivo geral desse trabalho é descrever os aspectos da trajetória de escolarização de crianças com lesão medular por mielomeningocele segundo a percepção de seus pais e professoras. Esse objetivo desdobrou-se nos seguintes objetivos específicos: destacar as peculiaridades da deficiência física no que diz respeito ao encaminhamento para inclus�
Publicado em: 2009
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3. Congenital hydrocehalus - a comparative study addressing maternal, gestational, perinatal and outcome characteristics of newborns with or without meningomyelocele / Estudo da evolução e prognostico comparativos de neonatos com hidrocefalia congenita isolada ou associada a defeitos do fechamento do tubo neural
Introdução: A hidrocefalia congênita é uma condição freqüente, estando associada a um terço de todas as malformações congênitas do sistema nervoso. O conhecimento clínico e epidemiológico da hidrocefalia congênita e dos variados fatores etiológicos e prognósticos a ela relacionados são até o momento insuficientes para a compreensão global
Publicado em: 2008
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4. Factors that interfere in clean intermittent catheterization (CIC) procedure in children with myelomeningocele under caregivers perception / Fatores interferentes na realização do cateterismo vesical intermitente em crianças com mielomeningocele na percepção do cuidador
This is an exploratory and descriptive research, primarily aiming at the analysis of factors that interfere in clean intermittent catheterization (CIC) procedure in children with neurogenic bladder, secondary to myelomeningocele (MMC), under caregivers perception. Fifty five 29-days-old to 11 years and 11 months-old children participated in the study. They w
Publicado em: 2005
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5. A Case of Meningomyelocele in a Kindred with Multiple Cases of Spondylolisthesis and Spina Bifida Occulta
A child with meningomyelocele, and other spinal anomalies, was born to a woman with three sibs who had spondylolisthesis and whose father and two of his sibs had a history of back problems. The suggestion is made that these anomalies represent a pattern of autosomal dominant inheritance with variable expressivity.
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6. Ophthalmic complications of meningomyelocele and hydrocephalus in children.
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7. Short report: Ventriculitis from Acinetobacter calcoaceticus variant anitratus
Ventriculitis from infection with Acinetobacter calcoaceticus variant anitratus occurred in an infant two weeks after surgical repair of a lumbosacral meningomyelocele and ventriculoperitoneal shunting. Recovery took place on replacing the shunt with an extraventricular deviation device and giving gentamicin and ampicillin intravenously.
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8. Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man.
A triploid fetus, 69, XXX, aborted spontaneously at 26 weeks' gestation. It had multiple abnormalities including syndactyly of the hands and feet single palmar creases, hypoplasia of the adrenals and ovaries, hypertrophy of thigh muscles, and abnormalities of the brain. The placenta was large and showed hydatidiform degeneration. The pregnancy had been compl
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9. A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome.
Neural tube defects (NTD) are among the most prevalent congenital malformations in man. Based on the molecular defect of Splotch, an established mouse model for NTD, and on the clinical association between NTD and Waardenburg syndrome (WS), mutations in the PAX3 gene can be expected to act as factors predisposing to human NTD. To test this hypothesis, 39 pat
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10. Measurement, Characterization, and Source of Somatostatin-like Immunoreactivity in Human Amniotic Fluid
Somatostatin-like immunoreactivity (SLI) is widely distributed in tissues and biological fluids. To determine whether SLI is also present in amniotic fluid, samples obtained by amniocentesis from 30 normal and 27 abnormal pregnancies were studied by radioimmunoassay. Direct incubation of [125I-Tyr1]tetradecapeptide somatostatin (SRIF) with amniotic fluid res