DYSTROPHIE MYOTONIQUE DE STEINERT PDF

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

We have examined literature about other affections for which fatigue were richly documented. You can move this seinert by clicking on the headline. Contact Help Who are we? Distinctions entre fatigue et somnolence dans la DM1.

Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

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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. Top of the page – Article Outline.

Literature review and research perspectives. La maladie de Steinert: Journal page Archives Contents list. 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. Outline Masquer le plan. Filleron bG. Access to the PDF text. Journal page Archives Contents list. Access to the text HTML.

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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. Ethical issues about the level of care, notably for tracheostomy and gastrostomy, should be adapted to each case, in partnership with parents.

At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy. Contact Help Who are we? If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.

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To better apprehend factors that may be involved in subjective fatigue in Steinert disease. La fatigue dans la dystrophie myotonique de Steinert: Fatigue is one of the depression symptoms.

Physical, mental and subjective fatigues are well known different types of fatigue. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.

If you want to subscribe to this journal, see our rates You can purchase this item dytsrophie Pay Per View: Access to the PDF text. Outline Masquer le plan.

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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.

Mesnage aA. Access to the text HTML. Montreuil b steiert, B. Two prognostic factors predict the risk of death in early infancy: If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: 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. 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.

Generalized hypotonia led to the diagnosis of the disease. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable myotnoique France, and not to disclose this data to third parties. Steinerf infant was extubated after 2 months.

Technical advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation. However, clinically, it seems ymotonique to try to understand those concepts separately, since they are highly intricate.