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Hydranencephaly in Association with Roberts Syndrome

Published online by Cambridge University Press:  18 September 2015

Chris E.U. Ekong  and
Bohdan Rozdilsky
Chris E.U. Ekong*
Affiliation:
Division of Neuropathology, University Hospital, Saskatoon, Canada
Bohdan Rozdilsky
Affiliation:
Division of Neuropathology, University Hospital, Saskatoon, Canada
*
Department of Neurosciences, University of Saskatchewan, Saskatoon, Canada S7N 0W8.
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Summary:

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A clinicopathological study in a case of Roberts syndrome (tetraphocomelia, cleft lip and palate, and phallic hypertrophy) is reported. This patient had hydranencephaly and imperforate anus, two additional congenital abnormalities so far not reported in this syndrome.

Type
Research Article
Information
Canadian Journal of Neurological Sciences , Volume 5 , Issue 2 , May 1978 , pp. 253 - 255
Copyright
Copyright © Canadian Neurological Sciences Federation 1978

References

REFERENCES

Appelt, H., Gerken, H., and Lenz, W. (1966). Telraphokomelie mit Lippen-Kiefer-Gaumenspalte und Clitoreshyper-trophie-ein Syndrom. Pädiatrie und Pädalogie. 2,119–124.Google Scholar
Freeman, M.V.R., German, J., Williams, D.W., Schimke, R.M., Temtamy, S.A., and Vachier, E. (1974). The Roberts Syndrome. Clin. Genet. 5: 1–16.CrossRefGoogle ScholarPubMed
Holmes, L.B., Moser, H.W., Hall-Dorson, S., Mack, C.Pant, S.S., Matzilevich, B. (1972). Mental Retardation. The MacMillan Company, New York. Pages 344 and 345.Google Scholar
Roberts, J.B. (1919). A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremities. Ann. Surg. 70, 252.Google Scholar