Apert syndrome: Diagnostic and management problems in a resource-limited country
Apert syndrome or acrocephalosyndactyly is a rare genetic disease characterized by craniofacial dysmorphism and syndactyly of the hands and feet. We report an observation in a 4-month-old female infant, whose father was 65 years old. The infant was admitted to the neonatology of Sourô Sanou Universi...
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2019-12-01
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| Series: | Pediatric Reports |
| Subjects: | |
| Online Access: | https://www.pagepress.org/journals/index.php/pr/article/view/8224 |