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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Clinical expression of myotonic dystrophy: Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Clin Genet, 23pp. Ultrasound Obstet Gynecol, 20pp. J Gynecol Obstet Biol Reprod, 24pp. Am J Med ; Pathologica, 84pp. Am J Obstet Gynecol,pp.

Arrhythmias conduction defects in myotonic dystrophy. Left ventricular relaxation, mitral valve prolapse and intracardiac conduction in myotonia atrophica: Semin Pediatr Neurol, 3pp. Cardiac abnormalities in myotonic dystrophy: Cardiac disease in myotonic dystrophy.


You can change the settings or fe more information by clicking here. Supression of ventricular tachycardia by sotalol in myotonic dystrophy. Cardiac disease in myotonic dystrophy Steinert’s disease: EEF identificou grupo de risco para implante de marcapasso. Uterine contractions during labor in myotonic muscular dystrophy.

Am J Cardiol ; Prog Cardiovasc Dis DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.

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

Tidsskr Nor Laegeforen,pp. Computations for prenatal prediction of myotonic dystrophy. Anaesth Intensive Care, 27pp. Grigg LE, Chan W et al.

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Mechanisms of sustained ventricular tachycardia in myotonic dystrophy: The movements of fetuses with congenital myotonic dystrophy in utero. Diseases of the heart and blood Vessels.

Distroria, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. J Am Coll Cardiol ; Myotonic dystrophy and pregnancy. A case report and recent literature. First-trimester prediction in fetus at risk for myotonic dystrophy. Prenat Diagn, 11pp.


Congenital myotonic dystrophy in Britain. Principios de medicina interna, pp.

Neurophysiol Clin, 21pp. Arch Dis Child, 54pp.

The heart in myotonia atrophica. Barber aI. Ventricular tachycardia and sudden death in myotonic dystrophy: J Am Coll Cardiol ; 6: J Okla State Med Assoc, 91pp. A neonatal case of congenital myotonic dystrophy. Anticipation in myotonic dystrophy. Arch Dis Child, 50pp.

Cardiac involvement in myotonic dystrophy. Ann Neurol, 35pp. J Med Genet, 29pp. Arch Dis Child, 67pp. Nenhum caso de taquicardia ventricular sustentada foi documentado. Myotonic dystrophy is an unusual entity, which is rarely associated with pregnancy due to the fact that those people who are affected usually present with genital atrophy and hypogonadism.

Congenital myotonic dystrophy [abstract].