Primary Ciliary Dyskinesia

CONCLUSION: PCD diagnosis is complex and requires integration of history, clinical picture, imaging, functional and structural analysis of motile cilia and, if available, genetic analysis to make a definitive diagnosis. It is critical that we continue to expand our knowledge of this group of rare disorders to improve the identification of PCD patients and to develop evidence-based therapeutic approaches.PMID:37516247 | DOI:10.1016/j.lpm.2023.104171

Source: Presse Medicale - July 29, 2023 Category: General Medicine Authors: Johanna Raidt Niki Tomas Loges Heike Olbrich Julia Wallmeier Petra Pennekamp Heymut Omran Source Type: research