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dc.contributor.authorShalet, Stephen M
dc.contributor.authorBeardwell, Colin G
dc.contributor.authorAarons, B M
dc.contributor.authorPearson, D
dc.contributor.authorMorris Jones, P H
dc.date.accessioned2012-01-04T22:52:05Z
dc.date.available2012-01-04T22:52:05Z
dc.date.issued1978-06
dc.identifier.citationGrowth impairment in children treated for brain tumours. 1978, 53 (6):491-4 Arch. Dis. Child.en
dc.identifier.issn1468-2044
dc.identifier.pmid686776
dc.identifier.doi10.1136/adc.53.6.491
dc.identifier.urihttp://hdl.handle.net/10541/200131
dc.description.abstractGrowth and growth hormone (GH) secretion were studied in 14 children with brain tumours before radiation and chemotherapy and at various time intervals afterwards. The peak GH response to hypoglycaemia was normal in all patients before radiation. In 6 patients the peak GH response was impaired 1 year after radiation, and in a seventh it was normal at 1 year but impaired 2 years after radiation. In 12 of 13 patients the growth velocity during the first year of chemotherapy was below the 3rd centile, although none of these had an initial standing height below the 3rd centile. Thus it appears that poor growth in such children occurs irrespective of whether radiation-induced GH deficiency develops. The cause of this impaired growth is unknown.
dc.language.isoenen
dc.subject.meshAdolescent
dc.subject.meshBrain Neoplasms
dc.subject.meshChild
dc.subject.meshChild, Preschool
dc.subject.meshFemale
dc.subject.meshGrowth Disorders
dc.subject.meshGrowth Hormone
dc.subject.meshHumans
dc.subject.meshInfant
dc.subject.meshInsulin
dc.subject.meshMale
dc.subject.meshSecretory Rate
dc.titleGrowth impairment in children treated for brain tumours.en
dc.typeArticleen
dc.contributor.departmentChristie Hospital, Withington, Manchester, M20 4BX, UKen
dc.identifier.journalArchives of Disease in Childhooden
refterms.dateFOA2020-04-20T14:10:31Z
html.description.abstractGrowth and growth hormone (GH) secretion were studied in 14 children with brain tumours before radiation and chemotherapy and at various time intervals afterwards. The peak GH response to hypoglycaemia was normal in all patients before radiation. In 6 patients the peak GH response was impaired 1 year after radiation, and in a seventh it was normal at 1 year but impaired 2 years after radiation. In 12 of 13 patients the growth velocity during the first year of chemotherapy was below the 3rd centile, although none of these had an initial standing height below the 3rd centile. Thus it appears that poor growth in such children occurs irrespective of whether radiation-induced GH deficiency develops. The cause of this impaired growth is unknown.


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