09 August 2021 : Case report
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
Rare disease
DOI: 10.12659/AJCR.932450
Am J Case Rep 2021; 22:e932450