Crouzon Syndrome with Ocular Abnormalities: A Case Report
Crouzon syndrome is a rare genetic disorder characterized by premature closure of cranial sutures, exophthalmos, beak-like nose and mid facial hypoplasia. It was initially described as hereditary syndrome of craniofacial synostosis. There is premature fusion of one or more cranial sutures in cranios...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
JCDR Research and Publications Pvt. Ltd.,
2016-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |