Congenital deafness (LOXHD1: c.5747G>C)
Congenital deafness in Rottweilers is a genetic disorder causing bilateral hearing loss from the first weeks of life. Affected puppies show profound deafness, without other apparent clinical signs.
This condition is associated with a mutation in the LOXHD1 gene, which plays a key role in the function of the cochlear hair cells.



