A Case of Primary Ciliary Aplasia Diagnosed by Nasal Biopsy
Primary ciliary aplasia is a rare congenital disease that alters normal function of the mucociliary apparatus. Patients generally present with severe, recurrent, or chronic airway infection. This report describes the ultrastructural alterations observed in the nasal mucosa of a 30-year-old female pa...
| Autores: | , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Universidad Pontificia Comillas ICAI-ICADE |
| Repositorio: | Repositori Obert UdL |
| OAI Identifier: | oai:repositori.udl.cat:10459.1/469553 |
| Acceso en línea: | https://doi.org/10.65396/ejra.1825504 https://hdl.handle.net/10459.1/469553 |
| Access Level: | acceso abierto |
| Palabra clave: | Ciliary aplasia Primary ciliary dyskinesia Ultrastructural study Sinusitis Bronchiectasis |
| Sumario: | Primary ciliary aplasia is a rare congenital disease that alters normal function of the mucociliary apparatus. Patients generally present with severe, recurrent, or chronic airway infection. This report describes the ultrastructural alterations observed in the nasal mucosa of a 30-year-old female patient who has suffered from chronic upper and lower respiratory tract infections since childhood. These ultrastructural features are consistent with complete ciliary aplasia, a rare form of primary ciliary dyskinesia. A high degree of suspicion for this disorder is mandatory for accurate diagnosis and prompt treatment. A careful description of the diagnostic procedures and treatment of this extremely rare disorder has been provided. |
|---|