A Comprehensive Approach for the Diagnosis of Primary Ciliary Dyskinesia—Experiences from the First 100 Patients of the PCD-UNIBE Diagnostic Center

Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respiratory symptoms usually start at birth. The lack of diagnostic gold standard tests is challenging, as PCD diagnostics requires different methods with high expertise. We founded PCD-UNIBE as the first c...

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Detalles Bibliográficos
Autores principales: Müller, Loretta, Savas, Sibel T., Tschanz, Stefan A., Stokes, Andrea, Escher, Anaïs, Nussbaumer, Mirjam, Bullo, Marina, Kuehni, Claudia E., Blanchon, Sylvain, Jung, Andreas, Regamey, Nicolas, Haenni, Beat, Schneiter, Martin, Ingold, Jonas, Kieninger, Elisabeth, Casaulta, Carmen, Latzin, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466881/
https://www.ncbi.nlm.nih.gov/pubmed/34573882
http://dx.doi.org/10.3390/diagnostics11091540

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466881/
https://www.ncbi.nlm.nih.gov/pubmed/34573882
http://dx.doi.org/10.3390/diagnostics11091540

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