La distrofia muscular es un trastorno genético que debilita de forma como enfermedad de Steinert: se trata del tipo distrofia muscular más frecuente en la.

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Continuing navigation will be considered as acceptance of this use. Myotonic distrkfia with no trinucleotide repeat expansion. Arch Dis Child, 67pp. A report of two cases and a review of the literature.

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. Dystrophia myotonica and pregnancy [abstract].


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Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Ultrasound Obstet Gynecol, 20pp. Arch Dis Child, 50pp.

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Distrofia muscular

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Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Plasencia aO.

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

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DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Today, molecular genetic myscular allow to make both prenatal and an early neonatal diagnosis. Myotonic dystrophy and pregnancy: J Okla State Med Assoc, 91pp. The myotony often worsens and obstetric complications increase; miscarriage, preterm delivery, hydrops fetalis, intrauterine death, difficulties in expulsion, intra and post partum muscuoar.

A case report and recent literature. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.