DISTROFIA MUSCULAR MIOTNICA DE STEINERT PDF

A distrofia miotônica (DM), também conhecida como doença de Steinert1,2 é a forma mais O diagnóstico de distrofia miotônica baseou-se na história familiar, .. Analysis of CTG repeat in skeletal muscle of myotonic dystrophy young and. Revista Española de Cardiología Insuficiencia cardíaca como manifestación cardiológica inicial de la distrofia miotónica de SteinertHeart Presentamos el caso de un varón de 36 años diagnosticado de distrofia muscular de Steinert cuya.

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Uterine contractions during labor in myotonic muscular dystrophy.

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

Left ventricular relaxation, mitral valve prolapse and intracardiac conduction in myotonia atrophica: Ultras Obstet Gyneacol [en prensa]. Pediatr Neurol, 12pp. J Okla State Med Assoc, 91pp. Arch Dis Child, 54pp. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. J Reprod Med, 28pp. Neurology, 42pp. 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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The movements of miotnia with congenital myotonic dystrophy in utero. Arrhythmias conduction defects in myotonic dystrophy. Identification of minimal expression of myotonic dystrophy using electroretinography. Analysis of CTG repeat in skeletal muscle of myotonic dystrophy young and adult patients: Hum Molec Genet ;4: Left ventricular myocardial function in myotonic dystrophy.

J Gynecol Obstet Biol Reprod, 24pp. Hospital Universitario Materno-Infantil de Canarias. Myotonic dystrophy with no trinucleotide repeat expansion.

Prenat Diagn, 11pp. Si continua navegando, consideramos que acepta su uso. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Cardiovasc Res ; Eur J Pediatr,pp.

How to cite this article. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. Obstet Gynecol, 42pp. A case report and recent literature.

Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Molecular basis of miotonic dystrophy: Relationships among electrophysiologic findings ditrofia clinical status, heart function, and extent of DNA mutation in myotonic dystrophy. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Semin Pediatr Neurol, 3pp. Acta Obstet Gynecol Scand, 65pp. Cardiac involvement in miohnica dystrophy.

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Ventricular tachycardica and sudden death in myotonic dystrophy. Neurophysiol Clin, 21pp. Prenat Diagn, 13pp.

Las Palmas de Gran Canaria. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.

The heart in myotonia atrophica. Congenital myotonic dystrophy [abstract]. The congenital form has a poor prognosis, and is more difficult to diagnose.

Congenital myotonic dystrophy in Britain. J Pediatr Ophthalmol Strabismus, 31pp. Ulster Med J, 63pp. Lancet, 2pp. Diagnostic problems in congenital myotonic dystrophy.

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Anaesth Intensive Care, 27pp. J Med Genet, 29pp. Pediatrie, 47pp. Cell, 68pp.