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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Contact Help Who are we? Congenital myotonic dystrophy type I in a very premature neonate: Access to the full text of this article requires a subscription. steinerh
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Steinert myotonic dystrophy is one of the most frequent adult hereditary myopathies. 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 steiner art 36 of that law your personal data.
The signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain. You can move this window by clicking on the headline. Access to the text HTML. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose dystrophke data to third parties.
Mesnage aA. Literature review and research perspectives. La maladie de Steinert: Access to the PDF text.
Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description
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: Fatigue in Steinert myotonic dystrophy: Outline Masquer le plan. We have examined literature about other affections for which fatigue were richly documented.
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The infant was extubated after 2 months. Gargiulo aM. 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.
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. If you are a subscriber, please sign ve ‘My Account’ at the top right of the screen.
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The potential impact of in vitro fertilization on disease expression may also be considered. Access to the text HTML.
Distinctions entre fatigue et somnolence dans la DM1. Contact Help Who are we?
Journal page Archives Contents list. Van Den Hende aS. 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.
If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. 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.