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.

Author: Zulkirr Mishura
Country: Burma
Language: English (Spanish)
Genre: Marketing
Published (Last): 11 December 2012
Pages: 297
PDF File Size: 6.98 Mb
ePub File Size: 20.32 Mb
ISBN: 446-1-47561-944-8
Downloads: 33182
Price: Free* [*Free Regsitration Required]
Uploader: Fauzuru

Persistent tunica vasculosa lentis as a sign of congenital myotonic dystrophy. Correlation of the myotonic syndrome in dystrophic and congenital myotonia. Complex relationships between clinical findings and structure of the GCT repeat. Uterine contractions during labor in myotonic dee dystrophy. Masui, 51pp. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy.

Clinical expression of myotonic dystrophy: Description of a case presenting with dysphagia. A neonatal case of congenital myotonic dystrophy. Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy. Electroencephalogr Clin Neurophysiol, 61pp.

  CHEMIA WODY I POWIETRZA GOMKA PDF

J Okla State Med Assoc, 91pp. Ned Tijdschr Geneeskd,pp.

Distrofia muscular

Pena-shokeir type I syndrome. DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.

Myotonic dystrophy and pregnancy. Principios de medicina interna, pp.

Ultrasound Obstet Gynecol, 20pp. Clin Genet, 23pp. Its association with pregnancy can lead to different problems. Arch Muscuoar Child, 67pp. Congenital myotonic dystrophy in Britain.

Distrofia muscular (para Padres)

Se continuar a navegar, consideramos que aceita o seu uso. Neurophysiol Clin, 21pp. 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.

Congenital myotonic dystrophy [abstract].

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

Am J Obstet Gynecol, 82pp. Molecular basis of miotonic dystrophy: Prenatal diagnosis of myotonic dystrophy by direct mutation analysis. A report of two cases and a review of the literature. Eur J Pediatr,pp.

Myotonic dystrophy with no trinucleotide repeat expansion. A study of ten cases. Neurology, 42pp. Diagnostic problems in congenital myotonic dystrophy. Are you a health professional able to prescribe or dispense drugs?