Cargando…
Pfeiffer syndrome in an adult with previous surgical correction: A case report of CT findings
Pfeiffer syndrome, affecting roughly 1 in 100,000 individuals is characterized by acrocephalosyndactyly – the premature closure of skull sutures (craniosynostosis). These acrocephalosyndactyly syndromes which are often sporadic de novo but also autosomal dominant in inheritance can be characterized...
| Autores principales: | , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2021
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8260745/ https://www.ncbi.nlm.nih.gov/pubmed/34257781 http://dx.doi.org/10.1016/j.radcr.2021.06.003 |