Merveille et al. (2011), described nine patients with Kartagener syndrome with homozygous (consanguineous patients) or compound heterozygous mutations on the CCDC39 gene. A similar phenotype has been reported in patients with CCDC39 or CCDC40 gene mutations (Blanchon et al., 2012). This evidence concerns the gene CCDC39 and Kartagener Syndrome.