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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Ulster Med J, 63pp. 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. Lancet, 2pp. Neonatal form of dystrophia myotonica.

First-trimester prediction in fetus at risk for myotonic dystrophy. Early electromyographic signs in congenital myotonic dystrophy. Anticipation in myotonic dystrophy.

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

Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy. Sleep apnea and respiratory dysfunction in congenital myotonic distrofiw. Tidsskr Nor Laegeforen,pp. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. A study of ten cases. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death.


Arch Dis Child, 50pp. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy.

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J Genet Hum, 28pp. Df Intensive Care, 27pp. Signs of fetal affectation during pregnancy are hydrops, hydramnios, a reduction in fetal movements, and a slow fetal heart rate. Clin Invest Ginecol Obstet, 25pp.

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Cell, 68pp. Pediatrie, 47pp. Hospital Universitario Materno-Infantil de Canarias. You can change the settings or obtain more information by clicking here. J Perinat Med, 24pp. Se continuar a navegar, consideramos que aceita o seu uso.

Barber aI. Are you a health professional able to prescribe or dispense drugs? The movements of fetuses with congenital myotonic dystrophy in utero. Complex relationships between clinical findings and structure of the GCT repeat.


Congenital myotonic dystrophy in Britain. Correlation of the myotonic syndrome in dystrophic and congenital myotonia.

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

Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.

Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. Clinical expression of myotonic dystrophy: Neurology, 42pp.

A report of two cases and a review of the literature. Diagnostic problems in congenital myotonic dystrophy. Prenatal diagnosis of myotonic dystrophy by direct mutation analysis. Clin Genet, 23pp. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.