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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Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie. Journal page Archives Contents list. Physical, mental and subjective fatigues are well known different types of fatigue. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, dystropie be used or stored, be corrected, clarified, updated or deleted. 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 data to third parties. Access to the PDF text. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
Congenital myotonic dystrophy type I in a very premature neonate: If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. We have examined literature about other affections for which fatigue were richly documented.
Technical advances in neonatal steinerr care now allow CDM1 children to survive prolonged ventilation.
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. Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology.
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Mesnage aA. 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. You can move this window by clicking on the headline. Outline Masquer le plan. Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies. You can move this window by clicking on the headline.
Montreuil bB. Two prognostic factors predict the risk of death in early infancy: Access to the PDF text.
Personal information regarding our website’s visitors, including their identity, is confidential. Literature review and research perspectives. La maladie de Steinert: Generalized hypotonia led to the diagnosis of the disease. 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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Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description
Access to the full text of this article requires a subscription. Journal page Archives Contents list. La fatigue dans la dystrophie myotonique de Steinert: If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Van Den Hende aS.
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The case of a week-old premature female infant, conceived by in vitro fertilization, is reported. Gargiulo aM. At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy. Filleron bG. To better apprehend factors that may be involved in subjective fatigue in Steinert disease. Personal information regarding steinerf website’s visitors, including their identity, is confidential.
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.
Contact Help Who are we? However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate.
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.