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La enfermedad de Steinert es una rara miopatía hereditaria caracterizada por debilidad muscular generalizada, miotonía y afección multisistémica. Aunque los . Download Citation on ResearchGate | Distrofia miotónica de Steinert | The complexity and variability of the manifestations of myotonic. PDF | La distrofia miotónica de Steinert (DM1) es una enfermedad hereditaria, caracterizada por desórdenes multisistémicos asociados a disfunción muscular.

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Arch Dis Child, 67pp. Dystrophia myotonica and pregnancy [abstract].

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

Neonatal form of dystrophia myotonica. Obstet Gynecol Surv, 41pp.

Barber aI. Obstetric complications as the first sign of myotonic dystrophy. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy. Anaesth Intensive Care, 27pp. J Perinat Med, 24pp. Curr Opin Neurol, 10pp. Its distrotia with pregnancy miogonica lead to different problems. Si continua navegando, consideramos que acepta su uso. First-trimester prediction in fetus at risk for myotonic dystrophy. Pediatr Neurol, 12pp.


Distrofia Miotonica de Steiner

Prenatal diagnosis of myotonic dystrophy by direct mutation analysis. Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. Clin Invest Ginecol Obstet, 25pp. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy.

J Genet Hum, 28pp. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Identification of distroofia expression of myotonic dystrophy using electroretinography.

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Ann Neurol, 35pp. Arch Dis Child, 54pp. Five cases in preterm babies and review of early reports.

Myotonic dystrophy with no trinucleotide repeat expansion. Acta Biomed Ateneo Parmense, 71pp.

Distrofia Miotonica de Steiner | Publish with Glogster!

Are you a health professional able to prescribe or dispense drugs? Cell, 68pp. Correlation of the myotonic syndrome in dystrophic and congenital myotonia. To improve our services and products, we use “cookies” own or third parties authorized to steonert advertising related to client preferences through the analyses of navigation customer behavior.

Pena-shokeir type I syndrome. Minerva Pediatr, 53pp. Ultras Obstet Gyneacol [en prensa]. Ultrasound Obstet Gynecol, 20pp. Obstet Gynecol, 42pp. A report of two cases and a review of the literature. Prenat Diagn, 13pp. Uterine contractions during labor in myotonic muscular dystrophy. J Reprod Med, 28pp. Molecular basis of miotonic dystrophy: Today, molecular genetic techniques allow to seinert both prenatal and an early neonatal diagnosis.


Specific molecular prenatal diagnosis for fe CTG mutation in myotonic dystrophy. Fetal akinesia deformation sequence. Lancet,pp. Recurrent hydramnios in association with myotonia dystrophica.

Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Electroencephalogr Clin Neurophysiol, 61pp.

You can change the settings or obtain more information by clicking here. Description of a case presenting with dysphagia. Plasencia aStienert. Anticipation in myotonic dystrophy.

Am J Obstet Gynecol, 82pp. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Hospital Universitario Materno-Infantil de Canarias.

Prenat Diagn, 11pp.