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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J Okla State Med Assoc, 91pp. Cell, 68pp. First-trimester prediction in fetus at risk for myotonic dystrophy.
Distrofia muscular (para Padres)
Neurology, 42pp. Molecular basis of miotonic dystrophy: Acta Biomed Ateneo Parmense, 71pp.
Clin Genet, 23pp. A neonatal case of congenital myotonic dystrophy. 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. Principios de medicina interna, pp.
Anal abnormalities in childhood myotonic dystrophy: Minimal somatic instability of CTG repeat in congenital myotonic dystrophy. Obstet Gynecol, 45pp. Obstetric complications as the first sign of myotonic dystrophy. Fetal akinesia deformation sequence. Tidsskr Nor Laegeforen,pp. Arch Dis Child, 50pp. Three times of anesthetic management in a patient with myotonic dystrophy [abstract].
The congenital form has a poor prognosis, and is more difficult to diagnose. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis. J Reprod Med, 28pp.
Ultras Obstet Gyneacol [en prensa]. Eguiluz aW. J Pediatr Ophthalmol Strabismus, 31pp. Prenatal diagnosis of myotonic dystrophy by musculad mutation analysis. Pena-shokeir type I syndrome. Congenital myotonic dystrophy [abstract].
Tent-shaped mouth as a presenting symptom of congenital myotonic dystrophy. Anaesth Intensive Care, 27pp. J Perinat Med, 24pp. Recurrent hydramnios in association with myotonia dystrophica. Uterine contractions during labor in myotonic muscular dystrophy. Ulster Med J, 63pp.
Am J Obstet Mscular, 82pp. Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion. 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.
Obstet Gynecol Surv, 41pp. J Gynecol Obstet Biol Reprod, 24pp. Nervenarzt, 70mucular. J Genet Hum, 28pp. Pathologica, 84pp.
Distrofia miotónica de steinert y gestación | Clínica e Investigación en Ginecología y Obstetricia
Ultrasound Obstet Gynecol, 20pp. Identification of minimal expression of myotonic dystrophy using electroretinography. Toko-Gin Pract, 61pp. Prenat Diagn, 11pp.
Electroencephalogr Clin Neurophysiol, 61pp. A study of ten cases. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Its association with pregnancy can lead to different problems. Antenatal and preoperative genetic and clinical assessment in myotonic dystrophy. The myotony often worsens and obstetric complications increase; miscarriage, preterm delivery, hydrops fetalis, intrauterine death, difficulties in steinwrt, intra and post partum haemorrhage.