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.

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You can move this window by clicking on the headline. Access to the PDF text. Ethical concertation about withdrawal or maintenance of intensive care was engaged, taking into account the prolonged ventilation, the degree of prematurity, and the parental wishes for maximum care.

Top of the page – Article Outline. Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies. Filleron bG.

Outline Masquer le plan. Contact Help Who are we?

Contact Help Who are we? At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy. The case of a week-old premature female infant, conceived by in vitro fertilization, is reported.

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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. Mesnage aA. Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology. Access to the full text of this article requires a subscription. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: La fatigue dans la dystrophie myotonique de Steinert: Top of the page – Article Outline.

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If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Gargiulo aM.

To better apprehend factors that may be involved in subjective fatigue in Steinert myotobique. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.

Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

We have examined literature about other affections for which fatigue were richly documented. The infant was extubated after 2 months.

Congenital myotonic dystrophy type I in a very premature neonate: Journal page Archives Contents list. Physical, mental and subjective fatigues are well known different types of fatigue. Literature on fatigue showed how relevant this trouble could be for a majority of patients; and also how specific fatigue could be steimert Steinert disease, compared to other neuromuscular pathologies: Access to the full text of this article requires a subscription.

Thus, more than in any other muscular diseases, factors that are not purely physical seem to be dystroophie in fatigue felt by patients with Steinert disease.

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Journal page Archives Contents list. Distinctions entre fatigue et somnolence dans la DM1. Literature review and research perspectives.

As per the Law relating to information storage and personal integrity, you have the right syeinert oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data. Access to the PDF text.

Two prognostic factors predict the risk of death in early infancy: Outline Masquer le plan. Technical advances in neonatal intensive care now allow Myotoniique 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.

As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data.