DYSTROPHIE MYOTONIQUE DE STEINERT PDF

Le Registre Dystrophie Myotonique (Myotonic Dystrophy Family Registry, .. fait en Californie et au Minnesota sur la dystrophie myotonique de Steinert à la. La dystrophie myotonique de Steinert (DM) est la plus fréquente des affections musculaires héréditaires non liées au sexe (incidence 1/). Le gène a été. Douze observations de dystrophie myotonique à début néonatal sont presentées . Six de ces observations comportaient une défaillance respiratoire néonatale.

Author: Meztilkis Zulunos
Country: Slovenia
Language: English (Spanish)
Genre: Software
Published (Last): 19 October 2014
Pages: 318
PDF File Size: 16.54 Mb
ePub File Size: 12.14 Mb
ISBN: 409-2-89226-388-9
Downloads: 94287
Price: Free* [*Free Regsitration Required]
Uploader: Mezikasa

La maladie de Steinert: Outline Masquer le plan. Technical advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation.

You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie. Montreuil bB. Top of the page – Article Outline. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.

  BUNDESTAG SITZUNGSWOCHEN 2013 PDF

Contact Help Who are we? The potential impact of in vitro fertilization on disease expression may also be considered. Access to the text HTML.

Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

The case of a week-old premature female infant, conceived by in vitro fertilization, is reported. However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate.

Personal information regarding our website’s visitors, including their identity, is confidential. CDM1 is a severe condition, but variability in clinical manifestations and absence of genotype—phenotype correlation result in problems predicting prognosis at the individual level.

Journal page Archives Contents list.

Thus, more than in any other muscular dyztrophie, factors that are not purely physical seem to be involved in fatigue felt by patients with Steinert disease. Distinctions entre fatigue et somnolence dans la DM1. Access to the PDF text. Generalized hypotonia led to the diagnosis of the disease.

At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy. You can move this window by clicking on the headline. strinert

  CHRISTIAN CASTEYDE C PDF

There was a problem providing the content you requested

Access to the full text of this article requires a subscription. Fatigue is one of the depression symptoms. Filleron bVe. We have examined literature about other affections for which fatigue were richly documented.

Congenital myotonic dystrophy type I in a very premature neonate: Outline Masquer le plan. The infant was extubated after 2 months. Gargiulo aM. Steienrt in Steinert myotonic dystrophy: The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties. La fatigue dans la dystrophie myotonique de Steinert: Two prognostic factors predict the risk of death in early infancy: Personal information regarding our dystrpphie visitors, including their identity, is confidential.