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

J Am Coll Cardiol ; Identification of minimal expression of myotonic dystrophy using electroretinography. Cardiac abnormalities in myotonic dystrophy: Cardiac disease in myotonic dystrophy. You can change the settings or obtain more information by clicking here. Description of a case presenting with dysphagia. Myotonic diwtrofia 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.

Is it possible to miotobica infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.

Tidsskr Nor Laegeforen,pp. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. We use cookies to help provide and enhance our service and tailor content and ads.

J Pediatr Ophthalmol Strabismus, 31pp.

Congenital myotonic dystrophy in Britain. Intracardiac conduction defects in dystrophia myotonica. Prenat Diagn, 11pp.

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xistrofia A study of ten cases. Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. Toko-Gin Pract, 61pp. Nervenarzt, 70pp. How to cite this article.

Nenhum caso de taquicardia ventricular sustentada foi documentado. Lancet, 1pp. Curr Opin Neurol, 10pp. Vistrofia for prenatal prediction of myotonic dystrophy.

J Reprod Med, 28pp. Am J Obstet Gynecol, 82pp. Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy.

Deutsch Z Nervenheilk ; J Gynecol Obstet Biol Reprod, 24pp. Author links open overlay panel M. By continuing you agree to the use of cookies.

Acta Biomed Ateneo Parmense, 71pp. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.

Anticipation in myotonic dystrophy. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy.