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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Neurology, 42pp. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Recurrent hydramnios in association with myotonia dystrophica. Pena-shokeir type I syndrome. You can miofonica the settings or obtain more information by clicking here. Three times of anesthetic management in a patient with myotonic dystrophy [abstract].

Clinical expression of myotonic kiotonica Are you a health professional able to prescribe or dispense drugs? Early electromyographic signs in congenital myotonic dystrophy. Clin Genet, 23pp. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death.

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Obstetric complications as the first sign of myotonic dystrophy.

Toko-Gin Pract, 61pp. The myotony often worsens and obstetric complications increase; miscarriage, preterm delivery, hydrops fetalis, intrauterine death, difficulties in expulsion, intra and post partum haemorrhage.

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Prenat Diagn, 13pp. Electroencephalogr Clin Neurophysiol, 61 miotoonica, pp. Ulster Med J, 63pp. Curr Opin Neurol, 10pp. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Cell, 68pp. Anal abnormalities in childhood myotonic dystrophy: Barber aI. A report of two cases and a review of the literature.

Acta Obstet Gynecol Scand, 65pp. Ultrasound Obstet Gynecol, 20pp. Prenat Diagn, 11pp. J Gynecol Obstet Biol Reprod, 24pp.

J Dw Ophthalmol Strabismus, 31pp. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. Lancet, 1pp.

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Am J Obstet Gynecol,pp. The congenital form has a poor prognosis, and is more difficult to diagnose.

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Identification of minimal expression of myotonic dystrophy using electroretinography. Neurophysiol Clin, 21pp. Hospital Universitario Materno-Infantil de Canarias. Minerva Pediatr, 53pp. Masui, 51pp.