Apert syndrome: A rare anomalad
Apert syndrome is a developmental malformation characterized by craniosynostosis, a cone shaped calvarium, midface hypoplasia, pharyngeal attenuation, ocular manifestations and syndactyly of the hands and feet. The complex craniofacial and systemic deformities seen in Apert syndrome mandate a multid...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Wolters Kluwer Medknow Publications,
2014-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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