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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Five cases in preterm babies and review of early reports. Prenat Diagn, 11pp. Continuing navigation will be considered as acceptance of this use. Cell, 68pp. Hospital Universitario Materno-Infantil de Canarias.

Ultrasound Obstet Gynecol, 20pp. Acta Obstet Gynecol Scand, 65pp. Neonatal form of dystrophia myotonica.

Distrofia Miotonica de Steiner | Publish with Glogster!

Computations for prenatal prediction of myotonic dystrophy. Ann Neurol, 35pp. Today, molecular genetic techniques allow to miotonicq both prenatal and an early neonatal diagnosis. Am J Obstet Gynecol,pp. J Okla State Med Assoc, 91pp. Myotonic dystrophy is an unusual entity, which is rarely associated with ce due to the fact that those people who are affected usually present with genital atrophy and hypogonadism.


A report of two cases and a review of the literature. 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.

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Ulster Med J, 63pp. Clin Genet, 23pp. Early electromyographic signs in congenital myotonic dystrophy.

Arch Dis Child, 67pp. Principios de medicina interna, pp. The myotony often worsens and obstetric complications increase; miscarriage, preterm delivery, hydrops fetalis, intrauterine death, difficulties in expulsion, intra and post partum haemorrhage. Eguiluz aW. The movements of fetuses with congenital myotonic dystrophy in utero. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. First-trimester prediction in fetus at risk for myotonic dystrophy.

Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Pathologica, 84pp. Dystrophia myotonica and pregnancy [abstract].


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Complex relationships between clinical findings and structure of the GCT repeat. Si continua navegando, consideramos que acepta su uso.

Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Van de Biezenbos, J. Anal abnormalities in childhood myotonic dystrophy: Obstet Gynecol, 45pp. Prenat Diagn, 13pp. Neurophysiol Clin, 21pp. Lancet,pp. Acta Biomed Ateneo Parmense, 71pp.

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

Its association with pregnancy can lead to different problems. Myotonic dystrophy and pregnancy. Molecular basis of miotonic dystrophy: Curr Opin Neurol, 10pp.