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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Clinical expression of myotonic dystrophy: Lancet, 1pp. Are you a health professional able to prescribe or dispense drugs?

You can change the settings or obtain more information by clicking here. J Reprod Med, 28pp. Congenital myotonic dystrophy in Britain.

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Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Pediatr Neurol, 12pp. Minerva Pediatr, 53pp.

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

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Its association with pregnancy can lead to different problems. Continuing navigation will be considered as acceptance of this use. The movements of fetuses with congenital myotonic dystrophy in utero.