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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Fatigue in Steinert myotonic dystrophy: If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Van Den Hende aS. Access to the text HTML. 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.

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: Motonique advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation.

To better apprehend factors that may be involved in subjective fatigue in Steinert disease.

We have examined literature about other affections for which fatigue were richly documented. Access to the PDF text.

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Access to the PDF text. La maladie de Steinert: 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.

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The potential impact of in vitro fertilization on disease expression may also be considered. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Ethical issues about the level of steinedt, notably for tracheostomy and gastrostomy, should be adapted to each case, in partnership with parents.

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. Top of the page – Article Outline. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Access to the full text of this article requires a subscription.

Personal information regarding our website’s visitors, including their identity, is confidential. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: The signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain.

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Generalized hypotonia led myotoniqus the diagnosis of the disease. Ethical concertation about withdrawal or maintenance of intensive care was engaged, taking into account the prolonged ventilation, the degree of prematurity, and dw parental wishes for maximum care. Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Myotonuque. Mesnage aA.

Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The infant was extubated after 2 months. Literature review and research perspectives.

Fatigue is one of the depression symptoms. You can move this window by clicking on the headline.

La fatigue dans la dystrophie myotonique de Steinert: Montreuil bB. The case of a week-old premature female infant, conceived by in vitro fertilization, is myotoniqje. Outline Masquer le plan.

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. Filleron bG.