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Apert syndrome or type I acrocephalosyndactyly

Case contributed by Hani Makky Al Salam
Diagnosis certain

Bilateral acrocephalosyndactyly

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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