Apert syndrome with frontonasal encephalocele
- 1 August 1985
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 21 (4) , 777-783
- https://doi.org/10.1002/ajmg.1320210422
Abstract
We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal encephalocele with unremarkable family history.Keywords
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