• The panel for hereditary Hearing Loss covers 160 genes. All of these genes are sequenced simultaneously. Only genes which have an association with the phenotype of the patient will be interpreted. For diagnostic purposes, each of the gene sets can be requested individually or in combination. A combination of individual genes is also possible.
    • Syndromic hearing loss
    • Non-syndromic, autosomal recessive and X linked
    • Non-syndromic, autosomal dominant and X linked