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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Ann Neurol, 35pp. Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the miotnkca form of myotonic dystrophy. Left ventricular relaxation, mitral valve prolapse and intracardiac conduction in myotonia atrophica: Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy.

Am Heart J ; A study of ten cases. Tidsskr Nor Laegeforen,pp. Minerva Pediatr, 53pp.

Continuing navigation will be considered as acceptance of this use. Ultrasound Obstet Gynecol, 20pp. J Gynecol Obstet Biol Reprod, 24pp.


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Cardiac disease in myotonic dystrophy Steinert’s disease: Obstetric complications as the first sign of myotonic dystrophy. 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.

Acta Obstet Gynecol Scand, 65pp. Nondystrophinopathic muscular dystrophies including myotonic dystrophy. EEF identificou grupo de risco para implante de marcapasso. Congenital myotonic dystrophy [abstract].

All the contents of this journal, except where otherwise noted, is licensed muscuar a Creative Commons Attribution License. Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods.

Molecular basis of myotonic dystrophy: Clinical expression of myotonic dystrophy: Radionuclide angiocardiographic analysis of myocardial function in myotonic muscular dystrophy.

Arrhythmias conduction defects in myotonic dystrophy.

Lancet, 1pp. Myotonyc Dystrophy, 2 nd edn. The movements of fetuses with congenital myotonic dystrophy in utero. Acta Biomed Ateneo Parmense, 71pp. Ventricular tachycardia steineft sudden death in myotonic dystrophy: DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.


Uterine contractions during labor in myotonic muscular dystrophy. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death.

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

Clinical classification of cardiac deaths. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy. Obstet Gynecol, 42pp.

Value of the electrocardiogram in determining cardiac events and mortality in myotonic dystrophy. Prenat Diagn, 13pp.

J Am Coll Cardiol ; Supression of ventricular tachycardia by sotalol in myotonic dystrophy. Obstet Gynecol Surv, 41pp.

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

Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy. Semin Pediatr Neurol, 3pp. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Molecular basis of miotonic dystrophy: Cardiac involvement in myotonic muscular dystrophy.