A distrofia miotônica (DM), também conhecida como doença de Steinert1,2 é a forma mais O diagnóstico de distrofia miotônica baseou-se na história familiar, .. Analysis of CTG repeat in skeletal muscle of myotonic dystrophy young and. Revista Española de Cardiología Insuficiencia cardíaca como manifestación cardiológica inicial de la distrofia miotónica de SteinertHeart Presentamos el caso de un varón de 36 años diagnosticado de distrofia muscular de Steinert cuya.

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Anal abnormalities in childhood myotonic dystrophy: Dystrophia myotonica and pregnancy [abstract]. Van de Biezenbos, J. The congenital form has a poor prognosis, and is more difficult to diagnose. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy.

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

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Molecular basis of miotonic dystrophy: Congenital myotonic dystrophy in Britain. Hospital Universitario Materno-Infantil de Canarias. Minerva Pediatr, 53pp. Masui, 51pp. Myotonic dystrophy and pregnancy: Toko-Gin Pract, 61pp. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. Clinical expression of myotonic dystrophy: Complex relationships between clinical findings and mionica of the GCT repeat.


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DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Diagnostic problems in congenital myotonic dystrophy. Neonatal myotonic dystrophy as muscupar cause of hydramnios and neonatal death.