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...

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Detalles Bibliográficos
Autores principales: Duggal, Neil, Omer, Adil, Jupalli, Sandhya, Pisinski, Leszek, Krauthamer, Alan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
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

Internet

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

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