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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Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy. Plasencia aDixtrofia. Services on Demand Journal. Br Heart J ; Pediatr Neurol, 12pp. Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. A report of two cases and a review of the literature.

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J Perinat Med, 24pp. EEF identificou grupo de risco para implante de marcapasso. Obstetric complications as the first sign of myotonic dystrophy. J Genet Hum, 28pp.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Mechanisms of sustained ventricular tachycardia in myotonic dystrophy: Anaesth Intensive Care, 27pp. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.

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

Distrotia, 51pp. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy. Barber aI. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy.

Five cases in preterm babies and review of early reports. Cardiac involvement in myotonic dystrophy.

Recurrent hydramnios in association with myotonia dystrophica. Uterine contractions during labor in myotonic muscular dystrophy.


Early electromyographic signs in congenital myotonic dystrophy. Congenital myotonic dystrophy in Britain. Ultrasound Obstet Gynecol, 20pp. Pathology of the cardiac conduction system in myotonic dystrophy: Analysis of CTG repeat in skeletal muscle of myotonic dystrophy young and adult patients: Las Palmas de Gran Canaria.

Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. A case report and recent literature. Neonatal form of dystrophia myotonica. Identification of minimal expression of myotonic dystrophy using electroretinography.

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

J Gynecol Obstet Biol Reprod, 24pp. Ann Neurol, 35pp. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.