2021
DOI: 10.12659/ajcr.932450
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Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages

Abstract: Patient: Female, 4-year-old Final Diagnosis: Pfeiffer syndrome Symptoms: Craniosynostosis • tracheal cartilage sleeves Medication: — Clinical Procedure: — Specialty: Pathology • Pediatrics and Neonatology Objective: Rare disease Background: Pfeiffer syndrome (PS) is a fibroblast growth factor receptor ( FGFR )-associated craniosynostosis syndrome, characterized by abnormal… Show more

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