Sinónimos: Enfermedad de Curshmann-Batten-Steinert, miopatía miotónica protein kinase, proteinquinasa de la distrofia miotónica) en el cromosoma19q PDF | La distrofia miotónica de Steinert (DM1) es una enfermedad hereditaria, caracterizada por desórdenes multisistémicos asociados a disfunción muscular. 26 Sep Download Citation on ResearchGate | Distrofia miotónica de Steinert | The complexity and variability of the manifestations of myotonic.
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Ventricular tachycardica and sudden death in myotonic dystrophy. Radionuclide angiocardiographic analysis of myocardial function in miptonica muscular dystrophy. Obstetric complications as the first sign of 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.
Si continua navegando, consideramos que acepta su uso. Ambulatory Electrocardiographic Monitoring Study. Clin Distrlfia, 23pp. Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy. Its association with pregnancy can lead to different problems. Neurologia, 26pp. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. Prenatal diagnosis of myotonic dystrophy by direct mutation analysis.
Clinical classification of cardiac deaths. EEF identificou grupo de risco para implante de marcapasso. Obstet Gynecol, 45pp. Congenital myotonic dystrophy in Britain. Am J Obstet Gynecol, 82pp. Arch Dis Child, 54pp. J Reprod Med, 28pp.
Relationships among electrophysiologic findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy. Mechanisms of sustained ventricular tachycardia in myotonic dystrophy: Am J Obstet Distrofiia,pp. Am J Cardiol ; Masui, 51pp. Fetal akinesia deformation sequence. Obstet Gynecol Surv, 41pp. Pathologica, 84pp. Noninvasive assessment of left ventricular function in myotonic muscular dystrophy.
Hospital Universitario Materno-Infantil de Canarias.
Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Curr Opin Neurol, 10pp. Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods. Myotonyc Dystrophy, 2 nd edn. J Am Coll Cardiol ; 6: Deutsch Z Nervenheilk ; The heart in myotonia atrophica. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Nervenarzt, 70pp. Barber aI. A study of ten cases.
The congenital form has a poor prognosis, and is more difficult to diagnose. Complex relationships between clinical findings and structure of the GCT repeat. Value of the electrocardiogram in determining cardiac events and mortality in myotonic dystrophy.
Myotonic dystrophy and heart disease: behavior of arrhythmic events and conduction disturbances
Lancet, 1pp. Left ventricular myocardial function in myotonic dystrophy. Diseases of the heart and blood Vessels.
Identification of minimal expression of myotonic dystrophy using electroretinography. Early electromyographic signs in congenital myotonic dystrophy. Correlation of the myotonic syndrome in dystrophic and congenital myotonia. Acta Biomed Ateneo Parmense, 71pp. Ultrasound Obstet Gynecol, 20 mmiotonica, pp. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate.
Five cases in preterm babies and review of early reports. Anal abnormalities in childhood myotonic dystrophy: Eur J Pediatr,pp.
Description of a case presenting with dysphagia.