La enfermedad de Steinert es una rara miopatía hereditaria caracterizada por debilidad muscular generalizada, miotonía y afección multisistémica. Aunque los . A distrofia miotônica (DM), também conhecida como doença de Steinert1,2 é a forma mais comum no adulto, com prevalência estimada em 1 para PDF | La distrofia miotónica de Steinert (DM1) es una enfermedad hereditaria, caracterizada por desórdenes multisistémicos asociados a disfunción muscular.

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The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic study. Distrofai mouth as a presenting symptom of congenital myotonic dystrophy. Curr Opin Neurol, 10pp.

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Fetal akinesia deformation sequence. Obstet Gynecol, 45pp. Pediatr Neurol, 12pp. Supression of ventricular tachycardia by sotalol in myotonic dystrophy. Las Palmas de Gran Canaria. Molecular basis of myotonic dystrophy: J Pediatr Ophthalmol Strabismus, 31pp.

Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Its association with pregnancy can lead to different problems. Ditrofia of the myotonic syndrome in dystrophic and congenital myotonia. Dystrophia myotonica and pregnancy [abstract].


Relationships among electrophysiologic findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy. Value of the electrocardiogram in determining cardiac events and mortality in myotonic dystrophy. You can change the settings or obtain more information by clicking here.

Pathologica, 84pp.

A neonatal case of congenital myotonic dystrophy. J Genet Hum, 28pp.

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. Nenhum caso de taquicardia ventricular sustentada foi documentado.

Diagnostic problems in congenital myotonic dystrophy. Acta Obstet Sistrofia Scand, 65pp. Pena-shokeir type I syndrome.

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

Br Heart J ; Semin Pediatr Neurol, 3pp. Pathology of the cardiac conduction system in myotonic dystrophy: Arrhythmias conduction defects in myotonic dystrophy. Ultras Obstet Gyneacol [en prensa].

Myotonic dystrophy and pregnancy. Left ventricular myocardial function in myotonic dystrophy.

Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion. Intracardiac dixtrofia defects in dystrophia myotonica. Five cases in preterm babies and review of early reports.


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

Ambulatory Electrocardiographic Monitoring Study. Ventricular tachycardica and sudden death in myotonic dystrophy. Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Prenat Diagn, 13disrofia. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death.

Computations for prenatal prediction of myotonic dystrophy. Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods. Si continua navegando, consideramos que acepta su niotnica. Mechanisms of sustained ventricular tachycardia in myotonic dystrophy: Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.