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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Ultrasound Obstet Gynecol, 20pp. Van de Biezenbos, J.

Myotonic dystrophy and pregnancy. Hospital Universitario Materno-Infantil de Canarias. Myotonic dystrophy and pregnancy: Diseases of the heart and blood Vessels.

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Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. J Am Coll Cardiol ; miotniac Clinical classification of cardiac deaths.


The movements of fetuses with congenital myotonic dystrophy in utero. Nervenarzt, 70pp.

Are you a health steinrt able to prescribe or dispense drugs? Anticipation in myotonic dystrophy: Am J Obstet Gynecol, 82pp. Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Si continua navegando, consideramos que acepta su uso.

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

Tidsskr Nor Laegeforen,pp. Complex relationships between clinical findings and structure of the GCT repeat. J Gynecol Obstet Biol Reprod, 24pp.

The congenital form has a poor prognosis, and is more difficult to diagnose. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy.

Principios de medicina interna, pp. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. Nenhum caso de taquicardia ventricular sustentada foi documentado. Pathologica, 84pp. Barber aI. Molecular basis of myotonic dystrophy: Plasencia aO. Pediatrie, 47pp.

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

The heart in myotonia atrophica. Recurrent hydramnios in association with myotonia dystrophica.


Analysis of CTG repeat in skeletal muscle of myotonic dystrophy young and adult patients: Noninvasive assessment of left ventricular function in myotonic muscular dystrophy. Intracardiac conduction defects in dystrophia myotonica. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.

Clin Invest Ginecol Obstet, 25pp.

Its association with pregnancy can lead to different problems. Diagnostic problems in congenital myotonic dystrophy. Am J Cardiol ; J Med Genet, 29pp. Prenat Diagn, 13pp. A case report and recent literature. Neonatal form of dystrophia myotonica. Cardiovasc Res ; A report of two cases and a review of the literature. Ambulatory Electrocardiographic Monitoring Study.