Primary Ciliary Dyskinesia

Defects in ciliated cells, particularly in the respiratory cilia

Symptoms
Recurrent infection of the upper and lower respiratory tract (sneezing, nasal discharge, cough and chronic bronchitis), hydrocephalus, reduced fertility in males

Gene involved
CCDC39

Mutation tested
c.286C>T

Transmission mode : Autosomal recessive

Publication : Merveille et al. (2011). CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.

Gene involved
NME5

Mutation tested
c.43delA

Transmission mode : Autosomal recessive

Publication : Anderegg et al. (2019). NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia.

Concerned breeds :