Figure 2From: A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome Clinical features of Apert syndrome in the patient. A, B. Note high flat skull (turribrachycephaly) associated with radiologically proven bicoronal synostosis. C-F. Note broad radially deviated thumbs, skin syndactyly of digits 2-4 in the hands and feet, and broad medially deviated great toes (C, post-operative after syndactyly release).Back to article page