DISTROFIA MUSCULAR DE STEINERT PDF

La distrofia muscular es un trastorno genético que debilita de forma como enfermedad de Steinert: se trata del tipo distrofia muscular más frecuente en la.

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DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis. Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Myotonic dystrophy with no trinucleotide repeat expansion. Anaesth Intensive Care, 27pp. Continuing navigation will be considered as acceptance of this use. Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion.

Lancet,muscuular. Cell, 68pp.

Distrofia muscular (para Padres)

Am J Obstet Gynecol, 82pp. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy.

A neonatal case of congenital myotonic dystrophy. Five cases in preterm babies and review of early reports. Lancet, 1pp. Las Palmas de Gran Canaria.

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Fetal akinesia deformation sequence. Pediatr Neurol, 12pp. You can change the settings or obtain stejnert information by clicking here. Clinical expression of myotonic dystrophy: Complex relationships between clinical findings and structure of the GCT repeat. Prenat Diagn, 13pp. Van de Biezenbos, J. Pathologica, 84pp.

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

Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Electroencephalogr Clin Neurophysiol, 61pp. Clin Genet, 23pp. Se continuar a navegar, consideramos que aceita o seu uso.

Obstetric complications as the first sign of myotonic dystrophy. Eguiluz aW.

Distrofia muscular

Pediatrie, 47pp. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy. Ned Tijdschr Geneeskd,pp.

Ultrasound Obstet Gynecol, 20pp. Correlation of the myotonic syndrome in dystrophic and congenital myotonia. Masui, 51pp. Curr Opin Neurol, 10pp. Nondystrophinopathic muscular dystrophies including myotonic dystrophy. Anal abnormalities in childhood myotonic dystrophy: First-trimester prediction in fetus at risk for myotonic dystrophy.