Significados de ciliary dyskinesia en inglés

The only demonstrable explanation for this patient's infertility was primary ciliary dyskinesia associated with KS.

Our results indicate that mutations in the TCTE3 gene are not a main cause of primary ciliary dyskinesia.

The estimated prevalence of primary ciliary dyskinesia in the UK South Asian population is 1:2265.

Rationale: Primary ciliary dyskinesia is a genetically heterogeneous inherited condition characterised by progressive lung disease arising from abnormal cilia function.

Methods: Next-generation sequencing was used to screen 86 South Asian patients who had a clinical history consistent with primary ciliary dyskinesia.