Should children with cerebral palsy and normal imaging undergo testing for inherited metabolic disorders?

Jane Leonard, Alison Cozens, Susan Reid, Michael Fahey, Michael Ditchfield, Dinah Reddihough

Research output: Contribution to journalArticleResearchpeer-review

Abstract

For the 9 to 16 of children with cerebral palsy (CP) who have normal brain imaging, further testing for metabolic and/or genetic conditions has been recommended. This study aimed to identify a cohort of children with CP with normal magnetic resonance imaging (MRI), clinically review and describe the cases, and assess the value to testing for inherited metabolic disorders in these children.
Original languageEnglish
Pages (from-to)226 - 232
Number of pages7
JournalDevelopmental Medicine and Child Neurology
Volume53
Issue number3
DOIs
Publication statusPublished - 2011

Cite this

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title = "Should children with cerebral palsy and normal imaging undergo testing for inherited metabolic disorders?",
abstract = "For the 9 to 16 of children with cerebral palsy (CP) who have normal brain imaging, further testing for metabolic and/or genetic conditions has been recommended. This study aimed to identify a cohort of children with CP with normal magnetic resonance imaging (MRI), clinically review and describe the cases, and assess the value to testing for inherited metabolic disorders in these children.",
author = "Jane Leonard and Alison Cozens and Susan Reid and Michael Fahey and Michael Ditchfield and Dinah Reddihough",
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Should children with cerebral palsy and normal imaging undergo testing for inherited metabolic disorders? / Leonard, Jane; Cozens, Alison; Reid, Susan; Fahey, Michael; Ditchfield, Michael; Reddihough, Dinah.

In: Developmental Medicine and Child Neurology, Vol. 53, No. 3, 2011, p. 226 - 232.

Research output: Contribution to journalArticleResearchpeer-review

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AU - Fahey, Michael

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AB - For the 9 to 16 of children with cerebral palsy (CP) who have normal brain imaging, further testing for metabolic and/or genetic conditions has been recommended. This study aimed to identify a cohort of children with CP with normal magnetic resonance imaging (MRI), clinically review and describe the cases, and assess the value to testing for inherited metabolic disorders in these children.

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