| Autor: |
DeGiovanni, C. V., Jong, C., Woollons, A. |
| Předmět: |
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| Zdroj: |
Pediatric Dermatology; Mar/Apr2007, Vol. 24 Issue 2, p186-188, 3p, 3 Color Photographs |
| Abstrakt: |
The article presents a case study of a then 13-year-old girl diagnosed with apert syndrome. Apert syndrome is a rare congenital type I acrocephalosyndactyly syndrome characterized by craniosynostosis, severe syndactyly of the hands and feet, and dysmorphic facial features. The patient was reported to have acne in three years duration. |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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