DISTROFIA MIOTONICA DE STEINERT PDF

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. PDF | La distrofia miotónica de Steinert (DM1) es una enfermedad hereditaria, caracterizada por desórdenes multisistémicos asociados a disfunción muscular.

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Diagnostic problems in congenital myotonic dystrophy. Plasencia aO.

Distrofia Miotonica de Steiner | Publish with Glogster!

Eur J Pediatr,pp. Nervenarzt, 70pp.

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A case report and recent literature. Prenat Diagn, 11pp. J Gynecol Obstet Biol Reprod, 24pp.

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You can change the settings or obtain more information by clicking here. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. A study of ten cases. Barber aI. Clin Invest Ginecol Obstet, 25pp. Electroencephalogr Clin Neurophysiol, 61pp. Toko-Gin Pract, 61pp.

Distrofia Miotonica de Steiner

A report of two cases and a review of the literature. Are you a health professional able to prescribe or dispense drugs? Obstetric complications as the first sign of myotonic dystrophy. Masui, 51pp. Hospital Universitario Tseinert de Canarias.

Anal abnormalities in childhood myotonic dystrophy: J Reprod Med, 28pp. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death.

Lancet,pp. Clin Genet, 23pp. Myotonic dystrophy is an unusual entity, which is rarely associated with pregnancy due to the stinert that those people who are affected usually present with genital atrophy and hypogonadism.

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

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