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Updated: Dec 23, 2025

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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.
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.
Area of Science:
- Genetics
- Pediatrics
- Craniofacial Anomalies
Background:
- Kenny-Caffey Syndrome Type 2 (KCS2) is a rare genetic disorder.
- It is characterized by short stature, skeletal dysplasia, primary hypoparathyroidism, and delayed anterior fontanelle closure.
- Patients often present with complex craniofacial and skeletal anomalies requiring multidisciplinary care.
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