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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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| Izdano u: | Radiol Case Rep |
|---|---|
| Glavni autori: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2021
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8260745/ https://ncbi.nlm.nih.gov/pubmed/34257781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.radcr.2021.06.003 |
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