SLN Otogenetics

Alport Syndrome
Aminoglycoside-Induced Deafness
Branchiootorenal Syndrome
Jervell and Lange-Nielson Syndrome
Pendred Syndrome
Sensorineural Hearing Loss
Stickler Syndrome
Treacher Collins Syndrome
Usher Syndrome
Waardenburg Syndrome
Zellweger Spectrum Disorders
Whole Exome Sequencing


SLN Otogenetics includes extensive list of genetic tests directed to the diagnostics of both non-syndromic and syndromic form of hearing loss and deafness.

Since accurate determination of the genetic diagnosis is complicated due to high genetic heterogeneity and phenotypic overlap, we have developed multi-gene screening panels for the detection of genetic causes of hereditary hearing loss.

Single-gene screening for GJB2 gene related disorders, Pendred Syndrome, and other forms of syndromic hearing loss is also available.

Differential diagnosis from different forms of hearing loss and deafness enables accurate genetic counseling and recurrence risk calculation, ensuring personalized care to the patients and their family members.