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The British Journal of Radiology, Vol 48, Issue 575 932-936, Copyright © 1975 by British Institute of Radiology
ARTICLES |
JO Haines and SC Rogers
A rare syndrome that can be diagnosed radiographically has been reviewed. A characteristic physiognomy, variable ophthalmologic anomalies and relatively specific dental and digital defects provide the diagnostic features. No hereditary component was identified and the chromosomal pattern was normal. The history, appearance and characteristic radiographic changes may, as in this case, allow the radiologist to provide a diagnosis not previously appreciated.
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