Families Of Children With Disability
Mostrando 13-21 de 21 artigos, teses e dissertações.
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13. Indivíduos com síndrome de Down: análise das principais repercussões sobre a saúde e a família
The Down Syndrome (DS) is the most frequent genetic cause of mental disability and has been hundreds of studies around the world focusing on clinical, epidemiological, cytogenetic and more recently genomics. This study had as main objective to describe the main sociodemographic characteristics of families of individuals with DS, affecting the health and inve
Publicado em: 2009
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14. Aspectos psicossociais de famílias de crianças com transtornos do desenvolvimento
Development disabilities (DD) are defined as "any nosologic entities or events of genetic origin or acquired by the first months of life, that undertake the development of the individual brain, and can cause disability, physical or mental, as well as restrictions on functionality and social participation." (Haase, Barreto &Freitas, in press). A literature re
Publicado em: 2008
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15. Elaboração e avaliação de um programa de intervenção psicopedagógico para orientação de pais de crianças com dificuldades de aprendizagem PPOP
Admission at the elementary school is an important moment in the process of education. Literature has shown that to guide the family in this process, using resources from the family environment, may be fundamental in preventing school problems. In that context, this work implemented and evaluated a proposal of intervention in the form of a Programa Psicopeda
Publicado em: 2008
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16. Care and the chronically ill patient: effects on the family structure / O cuidar e o paciente crônico: efeitos sobre a estrutura familiar
This work sought to understand how the family of chronically ill patients deals with them and how this care affects family structure. The main objective was to study changes in family relations due to caring for chronically disabled people 5 families responsible for severely mentally handicapped children, recruited in a specialized institution in Espírito S
Publicado em: 2007
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17. Identificação dos fatores associados ao atraso do desenvolvimento motor em crianças de um a quatro anos de idade com asma
Objective: To identify factors associated with delay in motor development, among children with asthma, from 1 to 4 years of age. Methods: Participated in this study 99 children with asthma who attended an assistential program named Criança que Chia, in Belo Horizonte, Minas Gerais. The mobility scale of the standardized Pediatric Evaluation of Disability In
Publicado em: 2006
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18. Buscando componentes da parceria colaborativa na escola entre família de crianças com deficiência e profissionais.
Professionals responsible for education of children with disabilities not always find the way to make their family a partner. This study aims to identify and describe the behaviors of professionals that work in the school and family members that are propitious and maintainers of the effective and successful collaborative partnership. The study was carried ou
Publicado em: 2006
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19. Prevalence and characteristics of disabled children: findings from the 1974 General Household Survey.
In the absence of nationally representative data on the prevalence of disability among children, a special analysis of relevant data in the General Household Survey (GHS) was carried out. A long-standing illness, disability or infirmity was present in 7.6% of the children under 16 in the 1974 sample of the GHS. An assessment of the extent to which the childr
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20. Social and emotional impact of faecal incontinence after surgery for anorectal abnormalities.
A significant proportion of children with anorectal malformations have long term problems with faecal continence. The psychological consequences of this chronic disability was assessed in 160 children and adolescents. The prevalence of clinically significant emotional problems among the sample overall, as assessed by a diagnostic psychiatric interview (19%),
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21. Holoprosencephaly in the west of Scotland 1975-1994.
Cases of holoprosencephaly which occurred in the west of Scotland over the past 20 years were ascertained from genetics, paediatric, and pathology department records. Fifty cases were identified of which 17 had an underlying cytogenetic abnormality. Of the remaining 33 cases, 26 were delivered after 28 weeks' gestation giving a birth prevalence of 1 in 26730