A case report describing insights into the imaging of Apert syndrome
Apert syndrome is a rare congenital autosomal dominant acrocephalosyndactyly type I syndrome which manifests in the form of various craniofacial, skeletal, and visceral anomalies. The present case reports this rare entity in a 15-month-old who presented with multiple craniofacial abnormalities, cran...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2024-01-01
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| Serie: | Rare |
| Soggetti: | |
| Accesso online: | http://www.sciencedirect.com/science/article/pii/S2950008724000061 |
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