Congenital deafness (LOXHD1: c.5747G>C)

€49.85
Test code: DOG-EOAD-ROTT
Analysis timeframe: 10 business days
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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.

Transmission

Autosomal recessive

Breed

Rottweiler

Gene

LOXHD1: c.5747G>C