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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. Distrofia miotónica o enfermedad de Steinert: estudio clínico-histopatológico de tres casos de una família. Arq. Neuro-Psiquiatr. [online]. , vol, n

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Recurrent hydramnios in association with myotonia dystrophica. Uterine contractions during labor in myotonic muscular dystrophy.

Las Palmas de Gran Canaria. Neurophysiol Clin, 21pp.

Pena-shokeir type I syndrome. Lancet, 1pp. Se continuar a navegar, consideramos que aceita o seu uso. Tidsskr Nor Laegeforen,pp.

Its association with pregnancy can lead to different problems.

Myotonic dystrophy and pregnancy: Acta Obstet Gynecol Scand, 65pp. Molecular basis of miotonic dystrophy: Toko-Gin Pract, 61pp. J Reprod Med, 28pp.


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

A case report and recent literature. Description of a case presenting with dysphagia. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy.

Prenatal diagnosis of myotonic dystrophy by direct mutation analysis. Acta Biomed Ateneo Parmense, 71pp. Continuing navigation will be considered as acceptance of this use.

Clin Genet, 23pp. Neonatal form of dystrophia myotonica. Neurologia, 26pp.

Ann Neurol, 35pp. Curr Opin Neurol, 10pp.

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Tent-shaped mouth as a presenting symptom 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.

Prenat Diagn, 13pp. Cell, 68pp. Semin Pediatr Neurol, 3pp. Eur J Pediatr,pp.

You can change the settings or obtain more information by clicking here. Clinical expression of myotonic dystrophy: Minerva Pediatr, 53pp. Electroencephalogr Clin Neurophysiol, 61pp.


Lancet, 2pp. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death. Ulster Med J, 63pp. Anticipation in myotonic dystrophy.

Barber aI. Identification of minimal expression of myotonic dystrophy using electroretinography. Anal abnormalities in childhood myotonic dystrophy: