Mental Retardation
Mostrando 1-12 de 693 artigos, teses e dissertações.
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1. Anxiety, attitudes-behaviors, coping styles, and social support among high-risk pregnant women in the late period of the coronavirus disease 2019 pandemic
SUMMARY OBJECTIVE: The purpose of this study was to investigate the prevalence of anxiety among high-risk pregnant women in the late period of the coronavirus disease 2019 pandemic and to evaluate the relationship between anxiety levels, attitudes-behaviors, coping styles, and other psychometric parameters. METHODS: Pregnant women who were followed up in o
Revista da Associação Médica Brasileira. Publicado em: 2022
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2. Occurrence of Dental Anomalies in Colombian Patients with Special Needs
Abstract Objective: To determine the occurrence of dental anomalies in patients with special needs from Barranquilla, Colombia. Material and Methods: An observational, cross-sectional descriptive study with a sample of 59 patients chosen at convenience for 6 months during the course of 2017. With prior approval by experts, an instrument that identified den
Pesqui. Bras. Odontopediatria Clín. Integr.. Publicado em: 10/10/2019
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3. A Novel Missense Mutation in SRD5A3 Causes Congenital Disorder of Glycosylation Type I (Cerebello-Ocular Syndrome)
Abstract A consanguineous Qatari family having an autosomal recessive disorder characterized by severe mental retardation, cerebellar vermis hypoplasia, retinal degeneration, optic nerve atrophy, ataxic gait, and seizures was studied for identification of the offending gene and mutation. Homozygosity mapping identified an 11.4 Mb critical interval at 4q12 to
J. inborn errors metab. screen.. Publicado em: 15/07/2019
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4. Adherence to Treatment of Phenylketonuria: A Study in Southern Brazilian Patients
Abstract Introduction: Phenylketonuria (PKU) is caused by the deficient activity of phenylalanine hydroxylase. Aim: To identify the factors associated with treatment adherence among patients with PKU seen at a southern Brazil reference center. Methodology: A cross-sectional, outpatient-based study including 56 patients with PKU (median age, 12 years) for
J. inborn errors metab. screen.. Publicado em: 19/06/2019
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5. WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities
RESUMO A aniridia é uma doença ocular congênita com grau variável de hipoplasia ou ausência do tecido da íris. É causada pela perda de função do gene PAX6 e pode ser uma anormalidade ocular isolada ou parte de uma síndrome. WAGRO refere-se a uma condição genética rara que leva ao tumor de Wilms, aniridia, anomalias geniturinárias, déficit inte
Arq. Bras. Oftalmol.. Publicado em: 20/05/2019
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6. Child and Adolescent Psychosocial Care Center service use profile in Brazil: 2008 to 2012
Objective: To describe the service use profile of Child and Adolescent Psychosocial Care Centers (Centro de Atenção Psicossocial Infanto-Juvenil [CAPSi]) in Brazil regarding diagnostic categories, sociodemographic aspects, and care modalities between 2008 and 2012. Methods: A descriptive, ecological study was performed using data from the Unified Health
Braz. J. Psychiatry.. Publicado em: 06/12/2018
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7. Caries experience and salivary aspects in individuals with fragile X syndrome
Abstract Fragile X syndrome (FXS) is the most common cause of hereditary mental retardation, but studies on the oral health condition of these patients are rare. The aim of this study was to determine the experience of dental caries in individuals with FXS, by examining the saliva profile, oral hygiene, socioeconomic characteristics and use of controlled dru
Braz. oral res.. Publicado em: 09/10/2017
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8. Onychogryphosis in tuberous sclerosis complex: an unusual feature
Abstract Onychogryphosis is an acquired nail plate change. It often affects the toenail and is characterized by an opaque, yellow-brownish nail plate that is distorted, grossly thickened, elongated, and partly curved resembling a ram's horn. Tuberous sclerosis complex is a multisystem disorder associated with high rates of mental retardation, autism, cogniti
An. Bras. Dermatol.. Publicado em: 2016-10
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9. Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
Introduction Auditory neuropathy/dyssynchrony (AN/AD) comprises a spectrum of pathology affecting the auditory pathways anywhere from the inner hair cells to the brainstem. It is characterized by an absent or atypical auditory brainstem response (ABR) with preservation of the cochlear microphonics and/or otoacoustic emissions (OAEs).
Int. Arch. Otorhinolaryngol.. Publicado em: 2015-06
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10. Homicide, fragile X syndrome, and mental retardation
Rev. Bras. Psiquiatr.. Publicado em: 2013-12
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11. Association of child maltreatment and psychiatric diagnosis in Brazilian children and adolescents
OBJECTIVES: The objective of this study was to evaluate the association between different types of child maltreatment and the presence of psychiatric disorders in highly vulnerable children and adolescents served by a multidisciplinary program. METHODS: In total, 351 patients with a mean age of 12.47, of whom 68.7% were male and 82.1% lived in shelters, u
Clinics. Publicado em: 2013
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12. Relação entre crimes sexuais e transtornos mentais e do desenvolvimento: uma revisão
CONTEXTO: A violência sexual é um grave problema de saúde pública que preocupa e confronta nossa sociedade. A prevalência, a magnitude e as consequências desse problema têm merecido atenção crescente por parte de estudiosos e pesquisadores da saúde e dos direitos humanos. OBJETIVO: Realizar uma revisão bibliográfica sobre a relação entre crimes
Arch. Clin. Psychiatry (São Paulo). Publicado em: 2013