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. 2024 Oct 28;10(5):00288-2024.
doi: 10.1183/23120541.00288-2024. eCollection 2024 Sep.

Questionnaire-assessed genotypes and associations with symptoms in primary ciliary dyskinesia

Eva S L Pedersen  1   2 , Myrofora Goutaki  1   3 , Leonie D Schreck  1   4 , Bernhard Rindlisbacher  5 , Lucy Dixon  6 , Jane S Lucas  7   8 , Claudia E Kuehni  1   3 ; COVID-PCD patient advisory group
Affiliations

Questionnaire-assessed genotypes and associations with symptoms in primary ciliary dyskinesia

Eva S L Pedersen et al. ERJ Open Res. .

Abstract

Collecting genetic information by questionnaire from people with PCD is feasible. This study confirmed typical differences in laterality defects and age at diagnosis between genotypes but found that symptoms were equally common across genotypes. https://bit.ly/4bvKW4R.

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Conflict of interest statement

Conflict of interest: The authors have nothing to disclose.

References

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