Kenny-Caffey Syndrome Type 2: A Unique Presentation and Craniofacial Analysis

Acara E Turner1, Amjed Abu-Ghname, Matthew J Davis

  • 1Division of Plastic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, and Division of Plastic Surgery, Texas Children's Hospital, Houston, TX.

Summary

Kenny-Caffey Syndrome Type 2 (KCS2) is a rare genetic disorder. This study reports the first identified case of craniosynostosis in a KCS2 patient, detailing associated craniofacial anomalies for early recognition.

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