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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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Obstet Gynecol, 45pp. Neurophysiol Clin, 21pp. A case report and recent literature. Clin Invest Ginecol Obstet, 25pp.

Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Myotonic dystrophy and pregnancy.

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Tidsskr Nor Laegeforen,pp. Computations for prenatal prediction of myotonic dystrophy. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. J Pediatr Ophthalmol Strabismus, 31pp. Neonatal form of dystrophia myotonica. Cell, 68pp. Myotonic dystrophy and pregnancy: Diagnostic problems in congenital myotonic dystrophy. Pathologica, 84pp. Fetal akinesia deformation sequence. steinerr


Arch Dis Child, 50pp. Clinical expression of myotonic dystrophy: A neonatal case of congenital myotonic dystrophy. Principios de medicina interna, pp. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy. Prenatal diagnosis of myotonic dystrophy by direct mutation analysis.

Lancet, 2pp. Recurrent hydramnios in association with myotonia dystrophica. J Med Genet, 29pp. Nervenarzt, 70pp. Plasencia aO. Obstet Gynecol Surv, 41pp. Continuing navigation will be considered as acceptance of this use.

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.

Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. Lancet, 1pp.

Acta Obstet Gynecol Scand, 65pp. Obstet Gynecol, 42pp. Dystrophia myotonica and pregnancy [abstract]. Se continuar a navegar, consideramos que aceita o seu uso. The congenital form has a distofia prognosis, and is more difficult to diagnose.

Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy.


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

Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. The movements of fetuses with congenital myotonic steiner in utero.

J Perinat Med, 24pp. Uterine contractions during labor in myotonic muscular dystrophy. Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy. Nondystrophinopathic muscular dystrophies including myotonic dystrophy.

Myotonic dystrophy with no trinucleotide repeat expansion. Neurology, 42pp. Ultras Obstet Gyneacol [en prensa]. Semin Pediatr Neurol, 3pp. Description of a case presenting with dysphagia. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy.

Toko-Gin Pract, 61pp. Am J Obstet Gynecol,pp.