Crouzon's syndrome: A case report and review
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformations. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the 1st year of life. Herein, we report a case of this rare entity, a 12-year-old girl with...
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| 主要な著者: | , , , |
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| フォーマット: | 図書 |
| 出版事項: |
Wolters Kluwer Medknow Publications,
2018-01-01T00:00:00Z.
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| 請求記号: |
A1234.567 |
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| 所蔵 1 | 利用可 |