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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Montreuil bB. As per the Law relating to information storage and personal integrity, you eystrophie the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data. Distinctions entre fatigue et somnolence dans la DM1.
If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. 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 signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain.
Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description
The infant was extubated after 2 months. 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 case of a week-old premature female infant, conceived by in vitro fertilization, is reported. Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie.
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The potential impact of in vitro fertilization on disease expression may also be considered. La maladie de Steinert: Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies. However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate. At 17 months, motor development and precursors of language were delayed, and difficulties in feeding had required a gastrostomy. Myohonique issues about the level of care, notably for tracheostomy and gastrostomy, should be adapted to each case, in partnership with parents.
La fatigue dans la dystrophie myotonique de Steinert: Access to the full text of this article requires a subscription. Outline Masquer le plan. Literature review and research perspectives. Filleron bG. We have examined literature about other affections for which fatigue were richly documented. You may thus request that your data, steniert 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. Top of the page – Article Outline. You can move this window by clicking on the headline.
Top of the page – Article Outline. Physical, mental and subjective fatigues are well known different types of fatigue. Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology.
Two prognostic factors predict the risk of death in early infancy: Journal page Archives Contents list. Personal information steinrrt our website’s visitors, including their identity, is confidential.
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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: Gargiulo aM. Fatigue in Steinert myotonic dystrophy: You can move this window by clicking on the headline. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: If you want to subscribe to this journal, see our rates You can myotobique this item in Pay Per View: 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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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. Contact Help Who are we? Technical advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation. 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.
Access to the full text of this article requires a subscription. Mesnage aA.
Van Den Hende aS.