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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However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate. La fatigue dans la dystrophie myotonique de Steinert: Ethical issues ydstrophie the level of care, notably for tracheostomy and gastrostomy, should be adapted to each case, in partnership with parents.
Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology. Physical, mental and subjective fatigues are well known different types of fatigue.
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If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies.
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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. Generalized hypotonia led to the diagnosis of the disease. Fatigue in Steinert myotonic dystrophy: At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy.
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You can move this window by dystrophid on the headline. 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. 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.
Montreuil bB. Literature on fatigue showed how relevant this trouble could be for a majority of patients; and also how specific steijert could be in Steinert disease, compared to other neuromuscular pathologies: Top of the page – Article Outline.
The signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain. The potential impact of in vitro fertilization on disease expression may also be considered. Literature review and research perspectives.
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.
To better apprehend factors that may be involved in subjective fatigue in Steinert disease.
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Filleron bG. Access to the PDF text. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, xteinert or deleted. 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 disease.
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Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description
If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Distinctions entre fatigue et somnolence dans la DM1. The case of a week-old premature female infant, conceived by in vitro fertilization, is reported. Outline Masquer le plan. Congenital myotonic dystrophy type I in a very premature neonate: Access to the full text myotoinque this article requires a subscription.
Contact Help Who are we? Two prognostic factors predict the risk of death in early infancy: Fatigue is one of the depression symptoms. Van Den Hende aS. Steinerf page Archives Contents list.
Outline Masquer le plan. Access to the text HTML. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The infant was extubated after 2 months. La maladie de Steinert: Personal information regarding our website’s visitors, including their identity, is confidential.