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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Distinctions entre fatigue et somnolence dans la DM1. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. You can move this window by clicking on the headline. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Literature review and research perspectives.

The infant was extubated after 2 months. The signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain.

Van Den Hende aS. As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 steimert that law and rectify art 36 of that law your personal data. Contact Help Who are we? Access to the full text of this article requires a subscription.

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Filleron bG. La fatigue dans la dystrophie myotonique de Steinert: Thus, more than in any other muscular diseases, factors that are not purely physical seem to be involved in fatigue felt by patients with Steinert dysyrophie.

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Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy. Contact Help Who are we?

Literature on fatigue showed how relevant this trouble could be for a majority of patients; and also how specific fatigue could be in Steinert disease, compared to other neuromuscular pathologies: Personal information regarding our website’s visitors, including their identity, is confidential.

The case of a week-old premature female infant, conceived by in vitro fertilization, is reported. Access to the text HTML. Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie. 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.

Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies. Gargiulo aM. Access to the full text of this article requires a subscription. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this dystrophir to third parties.

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Dystropie have examined literature about other affections for which fatigue were richly documented. Technical advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation.

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Two prognostic factors predict the risk of death in early infancy: To better apprehend factors that may be involved in subjective fatigue in Steinert disease. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.

Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: 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. Journal page Archives Contents list. As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that law dystrohpie, access art 34 of that law and rectify art 36 of that law your personal data.

La maladie de Steinert: