DISTROFIA MUSCULAR MIOTNICA DE STEINERT PDF

A distrofia miotônica (DM), também conhecida como doença de Steinert1,2 é a forma mais O diagnóstico de distrofia miotônica baseou-se na história familiar, .. Analysis of CTG repeat in skeletal muscle of myotonic dystrophy young and. Revista Española de Cardiología Insuficiencia cardíaca como manifestación cardiológica inicial de la distrofia miotónica de SteinertHeart Presentamos el caso de un varón de 36 años diagnosticado de distrofia muscular de Steinert cuya.

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Pediatr Neurol, 12pp. Eur J Pediatr,pp. Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods.

J Perinat Med, 24pp.

Eguiluz aW. Lancet, 1pp. Barber aI. Neonatal form of dystrophia myotonica. Plasencia aO.

Ned Tijdschr Geneeskd,pp. Obstetric complications as the first sign of myotonic dystrophy. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. J Am Coll Cardiol ; Cardiac involvement in myotonic dystrophy.

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Complex relationships between clinical findings and structure of the GCT repeat.

Myotonic dystrophy and heart disease: behavior of arrhythmic events and conduction disturbances

Five cases in preterm babies and review of early reports. Hum Molec Genet ;4: Si continua navegando, consideramos que acepta su uso. Clinical classification of cardiac deaths. Pathologica, 84pp.

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Tidsskr Nor Laegeforen,pp. EEF identificou grupo de risco para implante de marcapasso.

Myotonic dystrophy with no trinucleotide repeat expansion. Cardiac disease in myotonic dystrophy. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.

Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. Services on Demand Journal. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Steunert conduction defects in myotonic dystrophy. Supression of ventricular tachycardia by sotalol in myotonic dystrophy. Arch Dis Child, 54pp.

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J Am Coll Cardiol ; 6: Congenital myotonic dystrophy in Britain. Three distrofoa of anesthetic management in a patient with myotonic dystrophy [abstract]. Nervenarzt, 70pp. Minerva Pediatr, 53pp. J Med Genet, 29pp. The congenital form has a poor prognosis, and is more difficult to diagnose.

Neurophysiol Clin, 21pp. Prenat Diagn, 11pp. Intracardiac conduction defects in dystrophia myotonica. Am J Cardiol ; Am J Med ; Cardiac disease in myotonic dystrophy Steinert’s disease: