CROUZON SYNDROME - CLINICAL-EVOLUTIVE PARTICULARITIES. CASE REPORT
The Crouzon's Syndrome is a rare genetic disorder, with an incidence between 1/25,000 to 1/100,000 newborn babies, transmitted autosomal dominant, characterized by facial dysmorphism and craniosynostosis, based on those characteristic can be diagnosed early. We present the case of a premature n...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Amaltea Medical Publishing House,
2016-03-01T00:00:00Z.
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| 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 |