Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Sep 4;9(9):2871.
doi: 10.3390/jcm9092871.

Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress

Affiliations

Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress

Myrofora Goutaki et al. J Clin Med. .

Abstract

Neonatal respiratory distress (NRD) is common among infants with primary ciliary dyskinesia (PCD), but we do not know whether affected neonates receive a timely diagnosis. We used data from the international PCD cohort and assessed the proportion of patients with PCD who had a history of NRD and their age at diagnosis, stratifying by presence of laterality defects. First we analyzed data from all participants diagnosed after 2000, followed by individuals from a subgroup diagnosed using stricter criteria. Among the 1375 patients in the study, 45% had a history of NRD and 42% had laterality defects. Out of the 476 children with definite PCD diagnosis, 55% had a history of NRD and 50% had laterality defects. Overall, 30% of children with PCD were diagnosed during the first 12 months of life. This varied from 13% in those with situs solitus and no NRD, to 21% in those with situs solitus and NRD, 33% in those with situs anomalies but no NRD, and 52% in those with both situs anomalies and NRD. Our results suggest that we need to improve our knowledge of the neonatal presentation of infants with PCD and apply it so that these patients will receive appropriate care sooner.

Keywords: laterality defect; neonatal respiratory distress; orphan diseases; primary ciliary dyskinesia.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flow chart showing the patients included for the different analyses performed. PCD: primary ciliary dyskinesia.
Figure 2
Figure 2
Age at diagnosis of PCD patients (n = 476) aged 0–19 years with definite PCD diagnosis, per clinical characteristics group. PCD: primary ciliary dyskinesia, NRD: neonatal respiratory distress.

References

    1. Kuehni C.E., Frischer T., Strippoli M.P., Maurer E., Bush A., Nielsen K.G., Escribano A., Lucas J.S., Yiallouros P., Omran H., et al. Factors influencing age at diagnosis of primary ciliary dyskinesia in European children. Eur. Respir. J. 2010;36:1248–1258. doi: 10.1183/09031936.00001010. - DOI - PubMed
    1. Lucas J.S., Walker W.T., Kuehni C.E., Lazor R. Primary Ciliary Dyskinesia. Orphan Lung Dis. Eur. Respir. Monogr. 2011;54:201–217.
    1. O’Callaghan C., Chetcuti P., Moya E. High prevalence of primary ciliary dyskinesia in a British Asian population. Arch. Dis. Child. 2010;95:51–52. doi: 10.1136/adc.2009.158493. - DOI - PubMed
    1. Onoufriadis A., Paff T., Antony D., Shoemark A., Micha D., Kuyt B., Schmidts M., Petridi S., Dankert-Roelse J.E., Haarman E.G., et al. Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia. Am. J. Hum. Genet. 2013;92:88–98. doi: 10.1016/j.ajhg.2012.11.002. - DOI - PMC - PubMed
    1. Bequignon E., Dupuy L., Zerah-Lancner F., Bassinet L., Honore I., Legendre M., Devars du Mayne M., Escabasse V., Crestani B., Maitre B., et al. Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary Dyskinesia. J. Clin. Med. 2019;8:619. doi: 10.3390/jcm8050619. - DOI - PMC - PubMed