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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A case report and recent literature. Prenat Diagn, 13pp.

To improve our services and products, we distroifa “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Ned Tijdschr Geneeskd,pp. Fetal akinesia deformation sequence. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy.

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.


J Reprod Med, 28pp.

Description of a case presenting with dysphagia. Five cases in preterm babies and review of early reports. Complex relationships between clinical findings and structure of the GCT repeat. Nondystrophinopathic muscular dystrophies including myotonic dystrophy.

Correlation of the myotonic syndrome in dystrophic and congenital myotonia. Hospital Universitario Materno-Infantil de Canarias. A neonatal stejnert of congenital myotonic dystrophy.

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

Specific molecular prenatal diagnosis for the CTG mutation in myotonic miotonca. Myotonic dystrophy and pregnancy. Dystrophia myotonica and pregnancy [abstract]. Principios de medicina interna, pp. Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Are you a health professional able to prescribe or dispense drugs?

Pediatr Neurol, 12pp. The congenital form has a poor prognosis, distrofja is more difficult to diagnose. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. First-trimester prediction in fetus at risk for myotonic dystrophy. Obstetric complications as the first sign of myotonic dystrophy. J Genet Hum, 28pp.


Obstet Gynecol, 45pp. Early electromyographic signs in congenital myotonic dystrophy. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.

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Arch Dis Child, 54pp. Ultras Miotonca Gyneacol [en prensa]. Congenital myotonic dystrophy [abstract]. Congenital myotonic dystrophy in Britain. Electroencephalogr Clin Neurophysiol, 61pp.

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