Empowering limited-resource countries: collaborating with expert centers for diagnosis of primary ciliary dyskinesia

Empowering limited-resource countries: collaborating with expert centers for diagnosis of primary ciliary dyskinesia

IntroductionPrimary ciliary dyskinesia (PCD) is an autosomal recessive rare disease caused by alterations in ciliary structure and function. Without a unique gold standard diagnostic test, the European Respiratory Society and the American Thoracic Society recommend using various diagnostic technique...

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Main Authors: Mine Yuksel Kalyoncu, Rim Hjeij, Muruvvet Yanaz, Aynur Gulieva, Merve Selcuk Balcı, Şeyda Karabulut, Neval Metin Cakar, Almala Pınar Ergenekon, Ela Erdem Eralp, Yasemin Gokdemir, Heymut Omran, Bülent Taner Karadag
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Molecular Biosciences
Subjects:
primary ciliary dyskinesia (PCD)
international collaboration
low income countries
high speed video microscopy
rare disease
diagnostic challenges
Online Access:https://www.frontiersin.org/articles/10.3389/fmolb.2025.1547152/full
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https://www.frontiersin.org/articles/10.3389/fmolb.2025.1547152/full

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