Apert syndrome or type I acrocephalosyndactyly

Case contributed by Dr Hani Makky Al Salam

Bracycephaly and midface hypoplasia with premature fusion of the coronal suture and abnormal widening of the sagittal suture.

Note: This case has been tagged as "legacy" as it no longer meets image preparation and/or other case publication guidelines.

Case Discussion

Brachycephaly with coronal craniosynostosis, midface hypoplasia and multiple bilateral syndactyly in a patient with Apert syndrome.

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Case information

rID: 9731
Published: 16th May 2010
Last edited: 22nd Nov 2020
Inclusion in quiz mode: Included