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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Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Curr Opin Neurol, 10pp. Diagnostic problems in congenital myotonic dystrophy. Neurophysiol Clin, 21pp. Supression of ventricular tachycardia by sotalol in myotonic dystrophy.

Am J Cardiol ; Si continua navegando, consideramos que mootnica su uso. Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. A report of two cases and a review of the literature. Plasencia aO. Arch Dis Child, 67pp. Myotonyc Dystrophy, 2 nd edn. Se continuar a navegar, consideramos que aceita o seu uso. J Gynecol Obstet Biol Reprod, 24pp. Clin Genet, 23pp. Hospital Universitario Materno-Infantil de Canarias.


Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. Acta Biomed Ateneo Parmense, 71stsinert. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios.

The heart in myotonia atrophica. Anal abnormalities in childhood myotonic dystrophy: Arch Dis Child, 50pp.

Barber aI. EEF identificou grupo de risco para implante de marcapasso.

Noninvasive assessment of left ventricular function in myotonic muscular dystrophy. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Cardiac disease in myotonic dystrophy. Myotonic dystrophy is an unusual entity, tseinert is rarely associated with pregnancy due to the fact that those people who are affected usually present with genital atrophy and hypogonadism.

Eur J Pediatr,pp.

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

Services on Demand Journal. The movements of fetuses with congenital myotonic dystrophy in utero. J Genet Hum, 28pp. Anticipation in myotonic dystrophy: Five cases in preterm babies and review of early reports. Correlation of the myotonic syndrome in dystrophic and congenital myotonia.


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Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Nenhum caso de taquicardia ventricular sustentada foi documentado. Diseases of the heart and blood Vessels. Cardiovasc Res ; Neurology, 42pp. Lancet, 2pp. Continuing navigation will be considered as acceptance of this use. Neurologia, 26pp. J Am Coll Cardiol ; 6: Three times of anesthetic management in imotnica patient with myotonic dystrophy [abstract].

How to cite this article. Intracardiac conduction defects in dystrophia sgeinert. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy. Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods.