TABLE 4.
The Major Features of the Most Common Craniosynostosis Syndromes
| Apert | Crouzon | Pfeiffer | Muenke | Saethre-Chotzen | Carpenter | Craniofrontonasal dysplasia | |
| Synostosis coronal suture | + | + | + | + | + | + | + |
| Proptosis | + | + | |||||
| Ptosis | + | + | |||||
| Hypertelorism | + | + | + | + | + | ||
| Cleft palate | + | ||||||
| Deformity of the auricles | Small auricles with prominent auricular crura | ||||||
| Deformity of the hand | Complete syndactyly of dig 2–3–4, sometimes with 5 and or 1 | Broad thumbs Partial cutaneous syndactyly dig 2–3 | Partial cutaneous syndactyly dig 2–3 | Brachydactyly, clinodactyly, partial syndactyly, camptodactyly | Longitudinal grooves of the nails | ||
| Deformity of the foot | Complete syndactyly of all toes | Broad great toes; Partial cutaneous syndactyly dig 2–3–4 | Broad great toe in hallux valgus; Mild brachydactyly; Partial cutaneous syndactyly dig 3–4 | Duplicated great toe | Broad great toe; Longitudinal grooves of the nails | ||
| Malformations of the internal organs | 10% congenital heart defect; 10% urogenital malformation | 50% congenital heart defect, urogenital malformation (hypogenitalism) |