Work

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

Year: 2024

Type: article

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.

Source: Open Access CRIS of the University of Bern

DOI: 10.48620/76988

Authors: Pedersen, Eva S. L., Goutaki, Myrofora, Schreck, Leonie D., Rindlisbacher, Bernhard, Dixon, Lucy, Lucas, Jane S, Kuehni, Claudia E.

Institution: Institute of Social and Preventive Medicine

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W6911076029

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