Pfeiffer Syndrome Market: How Are Cranial Vault Distraction and Precision Genetic Diagnosis Transforming Craniofacial Surgery for FGFR-Related Craniosynostosis?
Pfeiffer syndrome — the autosomal dominant craniosynostosis disorder caused by mutations in FGFR1 and FGFR2, characterized by bicoronal synostosis, midface hypoplasia, broad thumbs and great toes, and variable digital syndactyly — represents one of the most technically demanding multidisciplinary conditions in pediatric surgery, with the Pfeiffer Syndrome Market reflecting the...
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