Abstract
A 6 year old white male was referred for evaluation of multiple congenital anomalies which included craniosynostosis, bony exostoses in the frontal and occipital regions, myopia, epibulbar dermoids, hearing loss and pigmented skin lesions. He does not appear to represent any of the recognized craniosynostosis syndromes.
Original language | English (US) |
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Pages (from-to) | 19-21 |
Number of pages | 3 |
Journal | Syndrome Identification |
Volume | 5 |
Issue number | 1 |
State | Published - Jan 1 1977 |
Externally published | Yes |
ASJC Scopus subject areas
- Medicine(all)