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...
Na minha lista:
| Principais autores: | , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2024-01-01
|
| Serier: | Rare |
| Fag: | |
| Online adgang: | http://www.sciencedirect.com/science/article/pii/S2950008724000061 |
| Tags: |
Ingen Tags, Vær først til at tagge denne postø!
|