Computed tomography assessment of Apert syndrome Avaliação da síndrome de Apert por meio da tomografia computadorizada
Apert syndrome, or acrocephalosyndactyly type I, is a craniofacial dysostosis, an autosomal dominant condition characterized by severe developmental disturbances of the craniofacial region including bilateral coronal synostosis associated with midface hypoplasia, exophthalmia, hypertelorism, and sym...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Sociedade Brasileira de Pesquisa Odontológica,
2004-03-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |