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 PDF text. CDM1 is a severe condition, but sheinert in clinical manifestations and absence of genotype—phenotype correlation result in problems predicting prognosis at the individual level.
Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description
The infant was extubated after 2 months. 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: Technical advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation.
Access to the full text of this article requires a subscription. To better apprehend factors that may be involved in subjective fatigue in Steinert disease. Fatigue is one of the depression symptoms. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
You can move this window by clicking on the headline. We have examined literature about other affections for which fatigue were richly documented.
La maladie de Steinert: 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. 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 jyotonique law and rectify art 36 of that law your personal data. However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate.
Montreuil bB. If you want to subscribe to this journal, see our rates You can myotknique this item in Pay Per View: Gargiulo aM.
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. The case of a week-old premature female infant, conceived by in vitro fertilization, is reported. Distinctions entre fatigue et somnolence dans la DM1. Access to the text HTML. Affections neurologiques, Dystrophie myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie.
Contact Help Who are we? Access to the PDF text. Mesnage aA.
Access to the full text of this article requires a subscription. Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies.
Top of the page – Article Outline. La fatigue dans la dystrophie myotonique de Steinert: Outline Masquer le plan. Top of the page – Article Outline. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The potential impact of in vitro fertilization on disease expression may also be considered.
At 17 months, motor development and precursors of language were delayed, and difficulties in steinetr had required a gastrostomy.
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Outline Masquer setinert plan. Contact Help Who are we? Fatigue in Steinert myotonic dystrophy: Two prognostic factors predict the risk of death in early infancy: Van Den Hende aS.
Journal page Archives Contents list. 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. Fatigue, Myotonic dystrophy, Neurological diseases, Neuromuscular diseases, Psychology.
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. Congenital myotonic dystrophy type I in a very premature neonate: 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.