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Jay P. Berke, MD; Kenneth R. Magee, MD

Arch Neurol. 1976;33(1):63-65.

Abstract
• A 16-year-old boy had craniofacial dysostosis, hydrocephalus, and syringomyelia. Other anomalies included platybasia, a Klippel-Feil anomaly, webbed toes, and a cutaneous hemangioma. Evaluation included cerebral angiography, ventriculography, and myelography.

Author Affiliations
From the Department of Neurology, University of Michigan Medical Center, Ann Arbor.

Footnotes
Accepted for publication Feb 18, 1975.

Reprint requests to the Department of Neurology, University of Michigan Medical Center, Ann Arbor, MI 48104 (Dr Magee).

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