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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Access to the text HTML. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Fatigue is one of the depression symptoms. Personal information regarding our website’s visitors, including their identity, is confidential. You can move this window by clicking on the headline. To better apprehend factors that may dysrophie involved in subjective fatigue in Steinert disease.

Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

Top of the page – Article Outline. Physical, mental and subjective fatigues are dystropihe known different types of fatigue. However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate. Fatigue in Steinert myotonic dystrophy: You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.

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Access to the full text of this article requires a subscription. Van Den Hende aS. Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology. The case of a week-old premature female infant, conceived by in steinerr fertilization, is reported. Outline Masquer le plan.

If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Journal page Archives Contents list. The infant was extubated after 2 months. At 17 months, motor development and dysfrophie of language were delayed, and difficulties in feeding had required a gastrostomy. Access to the text HTML.

Filleron bG. Montreuil bB. Outline Masquer le plan.

If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Access to the full text of this article requires a subscription. 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.

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Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Dyetrophie 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.

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The signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain. Access to the PDF text.

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. CDM1 is a severe condition, but variability in clinical manifestations and absence of genotype—phenotype correlation result myofonique problems predicting prognosis at the individual level.

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The potential impact of in vitro fertilization on disease expression may also be considered. Distinctions entre fatigue et somnolence dans la DM1. Mesnage aA. Generalized hypotonia led to the diagnosis of the disease. Ethical issues about the level of care, notably for tracheostomy and gastrostomy, should be adapted to each case, in partnership with parents.

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