Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure

Mieke Boon, Anne Smits, Harry Cuppens, Martine Jaspers, Marijke Proesmans, Lieven Dupont, F. Vermeulen, Sabine Van daele, Anne Malfroot, Véronique Godding,

Orphanet Journal of Rare Diseases · 2014 · 127 citations · 35 references

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Abstract

We reported on the clinical characteristics of a large population of patients with PCD and NU. We have shown that systematic performance of biopsy and cell culture increases sensitivity to detect PCD, especially the subtype with NU.PCD with NU has similar clinical characteristics as other PCD types and requires biopsy plus ciliogenesis in culture for optimal diagnostic yield.

References

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