Neurofibromatosis revisited : a pictorial review

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dc.contributor.author Khan, Nausheen
dc.contributor.author Van de Werke, Irma
dc.contributor.author Ismail, Farzanah
dc.date.accessioned 2010-05-21T12:32:54Z
dc.date.available 2010-05-21T12:32:54Z
dc.date.issued 2010-03
dc.description Because of the large number of images accompanying this review, and the cost of including them in the printed version of the journal, only the text has been published in print while the full review with all images appears on the open-access SAJR website http://www. sajr.org.za. Go to the site, click on Current, then on the image of ths issue’s front cover, and then on the title of this review on the contents page. en_US
dc.description.abstract Neurofibromatosis (or von Recklinghausen disease) is a hereditary condition due to mesodermal and neuroectodermal dysplasia, eponymously named after the researcher who reported it in 1882. The disorder is transmitted as an autosomal dominant condition, but 50% of cases arise as spontaneous mutations. The incidence falls within the range 1:2 000 - 1:4 000, and has no gender bias. We present a series of images produced by different modalities that show lesions and pathologies that are characteristic of the disease. en_US
dc.identifier.citation Khan, N, Van de Werke, I & Ismail, F 2010, 'Neurofibromatosis revisited : a pictorial review', SA Journal of Radiology, vol, 14, no. 1, pp. 16-18, 18a-18n. [http://www.journals.co.za/sama/m_sajr.html] en_US
dc.identifier.issn 1027-202X
dc.identifier.uri http://hdl.handle.net/2263/14084
dc.language.iso en en_US
dc.publisher Health & Medical Publishing Group en_US
dc.rights Health & Medical Publishing Group en_US
dc.subject Neurofibromatosis en_US
dc.subject Mesodermal en_US
dc.subject Neuroectodermal dysplasia en_US
dc.subject Eponymously en_US
dc.title Neurofibromatosis revisited : a pictorial review en_US
dc.type Article en_US


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