Crouzon Syndrome: a Comprehensive Review
Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying pathological process is premature synostosis of the cranial sutures with subsequent phenotypic alterations of the affected person. A review of the literature has been conducted in order to resume the over...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Balkan Stomatological Society,
2018-03-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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