DISTROFIA MUSCULAR MIOTNICA DE STEINERT PDF

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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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Electroencephalogr Clin Neurophysiol, 61pp.

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Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Masui, 51pp.

Left ventricular myocardial function in myotonic dystrophy. Am J Obstet Gynecol, 82pp. J Reprod Med, 28pp.

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

Fetal akinesia deformation sequence. Description of a case presenting with dysphagia. Eguiluz aW. Grigg LE, Chan W et al. Prenat Diagn, 11pp. J Perinat Med, 24pp.

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Principios de medicina interna, pp. Diagnostic problems in congenital myotonic dystrophy. Am J Med ; Cardiac involvement in myotonic muscular dystrophy.

Radionuclide angiocardiographic analysis of myocardial function in myotonic muscular dystrophy. A report of distfofia cases and a review of the literature. Dystrophia myotonica and pregnancy [abstract].

Ventricular tachycardica and sudden death in myotonic dystrophy. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate.

Acta Biomed Ateneo Parmense, 71pp. Se continuar a navegar, consideramos que aceita o seu uso. EEF identificou grupo de risco para implante de marcapasso. A case report and recent literature. Toko-Gin Pract, 61pp. Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion.

Diseases of the heart and blood Vessels. Congenital myotonic dystrophy [abstract]. Minerva Pediatr, 53pp. Five cases in preterm babies and review of early reports. Myotonic dystrophy with no trinucleotide repeat expansion. Molecular basis of myotonic dystrophy: Si continua navegando, consideramos que acepta su uso. All the contents distroia this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

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Semin Pediatr Neurol, 3pp.

Clin Invest Ginecol Obstet, 25pp. Neurologia, 26pp. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Myotonic dystrophy is an unusual entity, which is rarely associated with stelnert due to the fact that those people who are affected usually present dee genital atrophy and hypogonadism.

Relationships among electrophysiologic findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy. Ann Neurol, 35pp. J Genet Hum, 28pp. Arch Dis Child, 54pp. Arrhythmias conduction defects in myotonic dystrophy. First-trimester prediction in fetus at risk for myotonic dystrophy.