Please use this identifier to cite or link to this item: https://zone.biblio.laurentian.ca/handle/10219/101
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dc.contributor.authorYoung, Nancy-
dc.date.accessioned2007-11-02T16:17:52Z-
dc.date.available2007-11-02T16:17:52Z-
dc.date.issued2007-
dc.identifier.citationYoung NL. 2007. The transition to adulthood for children with cerebral palsy: what do we know about their health care needs? Journal of Pediatric Orthopaedics. Vol. 27(4).p.476-479.en_CA
dc.identifier.issn0 271 6798-
dc.identifier.urihttps://zone.biblio.laurentian.ca/dspace/handle/10219/101-
dc.descriptionFrom the Laurentian University, Sudbury, Ontario; The Hospital for Sick Children, Toronto, Ontario; and The Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.en_CA
dc.description.abstractThere have been significant changes in the clinical management of cerebral palsy (CP) during the past 2 decades. Gastrostomy tubes and nutritional supplements have been paramount in enhancing the life expectancy of those with CP. The literature shows that as many as 90% of children with CP can now expect to live to adulthood.1-4 As a result, CP is no longer considered to be a condition limited to childhood. However, emerging populations pose new challenges to those who provide health care support. This article presents an overview of what we know about the health care needs of adults with CP.en_CA
dc.description.sponsorshipDr Young is supported by a Canadian Institutes of Health Research Canada Research chair.en_CA
dc.language.isoenglishen_CA
dc.publisherLippincott Williams & Wilkinsen_CA
dc.subjectcerebral palsyen_CA
dc.subjectlife expectancyen_CA
dc.subjectnutritional supplementsen_CA
dc.subjecthealth care supporten_CA
dc.titleThe transition to adulthood for children with cerebral palsy: what do we know about their health care needs?en_CA
dc.typeArticleen_CA
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