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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
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 recept...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
International Scientific Literature, Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363655/ https://www.ncbi.nlm.nih.gov/pubmed/34366428 http://dx.doi.org/10.12659/AJCR.932450 |