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Abstract

The phakomatoses, or neuroectodermal dysplasias, are a group of hereditary conditions characterised by the development of tumours in many organs, but notably in the skin and CNS. A number of conditions have been included under this heading, but only five occur with sufficient frequency to merit our attention here, and of these I do not intend to discuss ataxia telangiectasia, as we have only scanned one of these patients, and the examination was unsatisfactory.

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References

  1. HORIE, A., SHIGEMI, V., FUKUSHIMA, T., TANAKA, K.: Neurofribromatosis complicated by intracranial tumours. Acta Pathologica Japonica 24, 705–716 (1974).

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© 1977 Springer-Verlag Berlin Heidelberg

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Kingsley, D.P.E. (1977). C.A.T. in the Phakomatoses. In: du Boulay, G., Moseley, I.F. (eds) The First European Seminar on Computerised Axial Tomography in Clinical Practice. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-66594-3_26

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  • DOI: https://doi.org/10.1007/978-3-642-66594-3_26

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-08116-6

  • Online ISBN: 978-3-642-66594-3

  • eBook Packages: Springer Book Archive

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