The importance of mdx mouse in the pathophysiology of Duchenne’s muscular distrophy. Arq. Neuro-Psiquiatr. [online]. , vol, n.3B, pp Importância do camundongo mdx na fisiopatologia da distrofia muscular de Duchenne. The importance of mdx mouse in the pathophysiology of Duchenne’s . Palavras-chave: Distrofia muscular de Duchenne, retardo mental, atraso do . Ao longo da história, os maiores focos da pesquisa sobre a fisiopatologia da.

Author: Nikozahn Tojajora
Country: Tanzania
Language: English (Spanish)
Genre: Finance
Published (Last): 15 December 2008
Pages: 339
PDF File Size: 20.20 Mb
ePub File Size: 15.35 Mb
ISBN: 516-8-52568-803-9
Downloads: 32990
Price: Free* [*Free Regsitration Required]
Uploader: Doushicage

O retardo mental na distrofia muscular de Duchenne. Distrofia muscular de Duchenne, retardo mental, atraso do desenvolvimento neuropsicomotor. To survey the medical literature directed musuclar the study of cognitive dysfunction in patients with Duchenne muscular dystrophy through description of the milestones of neurological development and psychometric tests for quantifying intelligence.

Non-systematic review of aspects of cognition in Duchenne muscular dystrophy in the major medical scientific bases: Patients with Duchenne muscular dystrophy exhibited delay in walking and language development, which correlated with lower scores on future intelligence tests. There is marked impairment in the verbal subtests. Average IQ has standard deviation below the average of the population.

The greater the cognitive impairment, the worse aspects related to morbidity and mortality in the disease will be. Duchenne muscular dystrophy, mental retardation, delay milestones, neurological development delay.

A DMD afeta um em cada 3.

O desenvolvimento neuropsicomotor na DMD. O desenvolvimento cognitivo na DMD. QI abaixo de ; RM grave: QI entre e ; RM moderado: QI entre e ; RM leve: O atraso neuropsicomotor ea DMD.

Com o acompanhamento da coorte de 22 pacientes com DMD feita por Parsons et al. De acordo com os resultados de Prosser et al. EmHinton et al. Enquanto alguns autores como Hinton et al. Emo grupo de Wingeier et al. De acordo com Cyrulnik et al. Conforme sugere Hinton et al. Segundo Mochizuki et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: Duchenne distrofis dystrophy and dystrophin: Segregation analysis of DMD families: Hoffman EP, Dressman D.


Molecular pathophysiology and targeted therapeutics for muscular dystrophy. Wrogemann K, Pena SD. Membrane protein kinase alteration in Duchenne muscular dystrophy. Neuromuscular disorders of infancy, childhood and adolescence.

The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy. Changes in spirometry over time as a prognostic marker in patients with Duchenne muscular dystrophy. Patterns and predictors of distrofiz disorders breathing in primary myopathies.

Fracture prevalence in Duchenne muscular dystrophy. Dev Med Child Neurol. Bone mineral density and fractures in boys with Duchenne muscular dystrophy. Brain Function in Duchenne muscular dystrophy.

Motor development in children with muscular dystrophy of the Duchenne type. Early development of boys with Duchenne muscular dystrophy.

Mental retardation in Duchenne muscular dystrophy

Developmental progress in Duchenne muscular dystrophy: Eur J Paediatr Neurol. Brain function in Duchenne muscular dystrofy.

Intelligence and Duchenne muscular dystrophy: Mental retardation in association with progressive muscular dystrophy. Am J Dis Child ; Intellectual functioning in Duchenne muscular dystrophy: Leibowitz D, Dubowitz V. Intellect and behavior in Duchenne muscular dystrophy. Intelligence and the gene for Duchenne muscular dystrophy.

Evidence for early impairment of verbal intelligence in Duchenne muscular dystrophy. Selective deficits in verbal working memory associated with a known genetic etiology: The neuropsychological profile of Duchenne muscular dystrophy. Dsitrofia cognitive deficits are common in children with Duchenne muscular dystrophy. Investigation of poor academic achievement in children with Duchenne muscular dystrophy. Learn Disabil Res Pract.


Verbal and memory skills in males with Duchenne muscular dystrophy. Cognitive and adaptive deficits in young children with Duchenne muscular dystrophy DMD. J Int Neuropsychol Soc.

Donders J, Taneja C.

Distrofia muscular

Neurobehavioral characteristics of children with Duchenne muscular dystrophy. Epub Jan Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne dichenne dystrophy.

Epub Nov Experimental tests of general intelligence. Mental retardation in the infant and pre-school child; diagnosis and treatment.


Kaminer RK, Jedrysek E. Age of walking and mental retardation. Am J Public Health. Possible risk factors and signs of mental retardation MR – comparative study of mentally retarded and normal children. ICD Guide for mental retardation. A rational approach to the child with mental retardation for the paediatrician. The epidemiology of mental retardation of unknown cause.

Mental retardation and lifetime events of Duchenne muscular dystrophy in Japan. Como citar este artigo: Mental retardation in Duchenne muscular dystrophy. J Pediatr Rio J. All the contents of this journal, except where otherwise noted, is licensed under a Creative Fisiopatollogia Attribution License.

Services on Demand Journal. Carlos Gomes, cj. How to cite this article.