Kartagener syndrome – the complexity of a primary ciliary dyskinesia phenotype and its rare association with cystic fibrosis: case report

References

Blouin JL, Meeks M, Radhakrishna U, Sainsbury A, Gehring C, Saïl GD, et al. Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity. European Journal of Human Genetics. 2000;8(2): 109–118. doi:10.1038/sj.ejhg.5200429
Open DOI Search in Google Scholar Back to article
Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, et al. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genetics in Medicine. 2009;11(7): 473–487. doi: 10.1097/GIM.0b013e3181a53562
Open DOI Search in Google Scholar Back to article
Afzeliuz BA, Stenram U. Prevalence and genetics of immotilecilia syndrome and left-handedness. The International Journal of Developmental Biology. 2006;50(6): 571–573. doi:10.1387/ijdb.052132ba
Open DOI Search in Google Scholar Back to article
Leigh MW, Zariwala MA, Knowles MR. Primary ciliary dyskinesia: improving the diagnostic approach. Current Opinion in Pediatrics. 2009;21(3): 320–325. doi:10.1097/MOP.0b013e328329cddb
Open DOI Search in Google Scholar Back to article
Leigh MW, O’Callaghan C, Knowles MR. The challenges of diagnosing primary ciliary dyskinesia. Proceedings of the American Thoracic Society. 2011;8(5): 434–437. doi:10.1513/pats.201103-028SD
Open DOI Search in Google Scholar Back to article