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FISIOTERAPIA NA DISTROFIA MUSCULAR DE DUCHENNE PDF

La Distrofia Muscular de Duchenne (DMD) es una enfermedad hereditaria do músculo, está localizado no braço curto do cromossomo X na região p21, pode. distrofia muscular de Duchenne: estudo de caso 4Curso de Fisioterapia do Departamento de Biomecânica, Medicina e Reabilitação do Aparelho Locomotor . OBJETIVO: A distrofia muscular de Duchenne é o tipo mais comum de miopatia genética. na experiência do autor em uma clínica pediátrica para tratamento de A maioria das crianças fazia sessões de fisioterapia regularmente, e seus.

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Os exames eram realizados por oculista ou oftalmologista. Os pacientes com uma grande variedade de miopatias podem ser afetados e eram alertados sobre esse risco antes de serem submetidos a cirurgia Os meninos com DMD e os adolescentes com DMB realizavam ecocardiogramas anuais para verificar sinais distrkfia de cardiomiopatia.

Update on the management of Duchenne muscular dystrophy.

Modern management of spinal muscular atrophy. Muscular Dystrophy Campaign [website]. Validity of the EK scale: The effects of knee-ankle-foot orthoses in the treatment of Duchenne muscular dystrophy: Glucocorticoid corticosteroids for Duchenne muscular dystrophy. Cochrane Database Syst Rev. Ciafaloni E, Moxley RT. Treatment options for Duchenne muscular dystrophy. Curr Treat Options Neurol. Congenital myasthenic syndromes in childhood: Forsyth R, Newton R.

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Serial casting of the ankles in Duchenne muscular dystrophy: Evolution of foot and ankle manifestations in children with CMT1A.

Surgery for scoliosis in Duchenne muscular dystrophy. A Dutch guideline for the treatment of scoliosis in neuromuscular disorders. Kotwicki T, Jozwiak M.

Conservative management of neuromuscular scoliosis: Orthopedic outcomes of long-term daily corticosteroid treatment in Duchenne muscular dystrophy. Deflazacort use in Duchenne muscular dystrophy: Risedronate for the prevention of bone mineral density loss in patients receiving high-dose glucocorticoids: Biphosphonate use and the risk of adverse jaw outcomes: J Am Dent Assoc. Tooth extraction socket healing in pediatric patients treated with intravenous pamidronate.

Cognitive impairment in neuromuscular disorders. Cognitive and psychological profile of males with Becker muscular dystrophy. Neuropsychiatric fisiotedapia in males with Duchenne muscular dystrophy: Sleep disorders in childhood-onset myotonic dystrophy type 1. Approved and investigational uses of modafinil: Hereditary sensory neuropathy type I.

Orphanet J Rare Dis. How many response levels do children distinguish on faces scales for pain assessment? Exploring chronic pain in youths with Duchenne Muscular Dystrophy: Clinch J, Eccleston C. Chronic musculoskeletal pain in children: Primary myopathies of the heart. Cardiovascular manifestations of myotonic dystrophy Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: Beneficial effects of beta-blockers and angiotensin-converting enzyme inhibitors in Duchenne muscular dystrophy.

Management of systemic hypertension in children and adolescents: Curr Treat Options Cardiovasc Med. The multidisciplinary management of Duchenne muscular dystrophy.

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DUCHENNE BECKER

Pulmonary rehabilitation in patients with neuromuscular disease. Mechanical insufflation-exsufflation for airway mucus clearance. Robert D, Argaud L. Swallowing difficulties in Duchenne muscular dystrophy: Eur J Paediatr Neurol.

distrofia muscular progresiva: Topics by

Oral health in children and adolescents with myotonic dystrophy. Eur J Oral Sci. Currently recommended treatments of childhood constipation are not evidence based: Feeding problems in merosin deficient congenital muscular dystrophy.

Feeding problems and malnutrition in spinal muscular atrophy type II. Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy.

J Clin Neuromuscul Dis. Ellsworth P, Caldamone A. Do systemic symptoms predict the risk of kidney scarring after urinary tract infection? Transition from pediatric to adult care: Approaching a new duchenne in Duchenne muscular dystrophy treatment.

Como citar este artigo: Long-term management of children with neuromuscular disorders. J Pediatr Rio J.

Long-term management of children with neuromuscular disorders

All the contents of this journal, except where otherwise noted, is licensed under a Distroffia Commons Attribution License. Services on Demand Journal. Carlos Gomes, cj. How to cite this article.