DISTROFIA 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. 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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DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Semin Pediatr Neurol, 3pp. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios.
Lancet,pp. Myotonic dystrophy is an unusual entity, which is rarely associated with pregnancy due to the fact that those people who are affected usually present with genital atrophy and hypogonadism.
Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Cell, 68pp.
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Clinical expression of myotonic dystrophy: Congenital myotonic dystrophy [abstract]. Si continua navegando, consideramos que acepta su uso.
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Distrofia miotónica de steinert y gestación | Clínica e Investigación en Ginecología y Obstetricia
Acta Obstet Gynecol Scand, 65pp. 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. J Perinat Med, 24pp. Computations for prenatal prediction of myotonic dystrophy.
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Las Palmas de Gran Canaria.