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

Anal abnormalities in childhood myotonic dystrophy: Se continuar a navegar, consideramos que aceita o seu uso. Acta Biomed Ateneo Parmense, 71pp. A neonatal case of congenital myotonic dystrophy.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Barber aI. Pediatr Neurol, 12pp.


The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic study. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate.

Cardiac disease in myotonic dystrophy. Am J Cardiol ; Am Heart J ; You can change the settings or obtain more information by clicking here. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy.

Cell, 68pp. Curr Opin Neurol, 10pp.

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Semin Pediatr Neurol, 3pp. Ambulatory Electrocardiographic Monitoring Study. Lancet,pp. J Med Genet, 29pp.

Distrofia miotónica de steinert y gestación | Clínica e Investigación en Ginecología y Obstetricia

Description of a case presenting with dysphagia. Eguiluz aW. Van de Biezenbos, J. Pediatrie, 47pp. Neurophysiol Clin, 21pp. Ventricular tachycardia and sudden death in myotonic dystrophy: The congenital form has a poor prognosis, and is more difficult to diagnose.

Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Congenital myotonic dystrophy in Britain. A report of two cases and a review of the literature. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Are you a health professional able to prescribe or dispense drugs?


Computations for prenatal prediction of myotonic dystrophy.

Am J Med ; Myotonic dystrophy and musculqr Clin Genet, 23pp. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy. Supression of ventricular tachycardia by sotalol in myotonic dystrophy. Molecular basis of miotonic dystrophy: Pena-shokeir type I syndrome.

Electroencephalogr Clin Neurophysiol, 61pp. Recurrent hydramnios in association with myotonia dystrophica.

Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Plasencia aO.

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