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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J Pediatr Ophthalmol Strabismus, 31pp. A case report and recent literature.

Am J Obstet Gynecol, 82pp. Barber aI. Myotonic dystrophy and pregnancy.

Pediatrie, 47pp. A study of ten cases. Plasencia aO. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy.

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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 distrfoia hypogonadism. Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death. Anaesth Intensive Care, 27pp. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios.

Pathologica, 84pp.

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

DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Description of a case presenting with dysphagia. Se continuar a navegar, consideramos que aceita o seu uso. Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Eur Dostrofia Pediatr,pp. Obstet Gynecol, 42pp.

The myotony often worsens and obstetric complications increase; miscarriage, preterm delivery, hydrops fetalis, intrauterine death, difficulties in expulsion, intra and post partum haemorrhage.

Three times of anesthetic management in a patient with myotonic dystrophy [abstract]. Congenital myotonic dystrophy [abstract].

Continuing navigation will be considered as acceptance of this use. Diagnostic problems distrogia congenital myotonic dystrophy. Myotonic dystrophy with no trinucleotide repeat expansion. Acta Biomed Ateneo Parmense, 71pp.

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J Okla State Med Assoc, 91pp. Ann Neurol, 35pp. Tidsskr Nor Laegeforen,pp. Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy.

Neurology, 42pp. Prenat Diagn, 11pp. Pediatr Neurol, steinrrtpp. J Perinat Med, 24pp. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy.

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Prenat Diagn, 13pp. Identification of minimal expression of myotonic dystrophy using electroretinography. Neurologia, 26pp. Steniert aW. Correlation of the myotonic syndrome in dystrophic and congenital myotonia.