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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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. Uterine contractions during labor in myotonic muscular dystrophy. Pathologica, 84pp. Ann Neurol, 35pp.

Prenat Diagn, 13pp. Cell, 68pp. Curr Opin Neurol, 10pp. Nondystrophinopathic muscular dystrophies including myotonic dystrophy.

Obstetric complications as the first sign of myotonic dystrophy. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death. Barber a distroifa, I. First-trimester prediction in fetus at risk for myotonic dystrophy. Obstet Gynecol, 45pp. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy. Anticipation in myotonic dystrophy.


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Anaesth Intensive Care, 27pp. Recurrent hydramnios in association with myotonia dystrophica.

J Pediatr Ophthalmol Strabismus, 31pp. Hospital Universitario Materno-Infantil de Canarias. Clinical expression of myotonic dystrophy: Am J Obstet Gynecol, 82pp. 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.

Ultras Obstet Gyneacol [en prensa]. Dystrophia myotonica and pregnancy [abstract]. Complex relationships between clinical findings and structure of the GCT repeat.

Distrofia Miotonica de Steiner

J Gynecol Obstet Biol Reprod, 24pp. Se continuar a navegar, consideramos que aceita o seu uso. A neonatal case of congenital myotonic dystrophy. The congenital form has a poor prognosis, and is more difficult to diagnose. Anal abnormalities in childhood myotonic dystrophy: Pediatrie, 47pp.

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Neurophysiol Clin, 21pp. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a distrrofia fetal heart rate. Molecular basis of miotonic dystrophy: Five cases in preterm babies and review of early reports.


J Med Genet, 29pp. Si continua navegando, consideramos que acepta su uso.

Its dd with pregnancy can lead to different problems. Minerva Pediatr, 53pp. J Reprod Med, 28pp. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Eguiluz aW. The movements of fetuses with congenital myotonic dystrophy in utero.

Early electromyographic signs in congenital myotonic dystrophy.

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

Toko-Gin Pract, 61pp. Lancet, 1pp. Ned Tijdschr Geneeskd,pp. Semin Pediatr Neurol, 3pp. Neonatal form of dystrophia myotonica. Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy.

Correlation of the myotonic syndrome in dystrophic and congenital myotonia. Van de Biezenbos, J. Are you a health professional able to prescribe or dispense eistrofia

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