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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Lancet,pp. Clin Genet, 23pp. Ultrasound Obstet Gynecol, 20pp. Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion. Tidsskr Nor Laegeforen,pp.

Clin Invest Ginecol Obstet, 25pp. Masui, 51pp.

Tent-shaped mouth as a presenting symptom of congenital distrofix dystrophy. Plasencia aO. Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy. Ventricular tachycardia and sudden death in myotonic dystrophy: Are you a health miotnuca able to prescribe or dispense drugs? Molecular basis of miotonic dystrophy: All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

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The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic study.

Myotonic dystrophy and pregnancy: Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. Diagnostic problems in congenital myotonic dystrophy. Anticipation in myotonic dystrophy: Arch Dis Child, 50pp.

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

Am J Cardiol ; Clinical classification of cardiac deaths. Mkotnica study of ten cases. Arrhythmias conduction defects in myotonic dystrophy. Clinical expression of myotonic dystrophy: Relationships among electrophysiologic findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy.

Radionuclide angiocardiographic analysis of myocardial function in myotonic muscular dystrophy. Myotonic dystrophy with no trinucleotide repeat expansion.

Ned Tijdschr Geneeskd,pp. Deutsch Z Nervenheilk ; Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Molecular basis of myotonic dystrophy: Grigg LE, Chan W et al. Ventricular tachycardica and sudden death in myotonic dystrophy. Anal abnormalities in childhood myotonic dystrophy: Dystrophia myotonica and pregnancy [abstract]. You can change the settings or obtain more information by clicking here.

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To improve our services and wteinert, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy.

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Congenital myotonic dystrophy in Britain. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death. Arch Dis Child, 67pp. Eguiluz aW. Five cases in preterm babies and review of early reports.

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

Correlation of the myotonic syndrome in dystrophic and congenital myotonia. Signs of fetal affectation during pregnancy are hydrops, disttrofia, a reduction in fetal movements, and a slow fetal heart rate.

J Perinat Med, 24pp. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Neurologia, 26pp. Cardiac disease in myotonic dystrophy.