OtoSCOPE® Genetic Hearing Loss Testing

The BEST comprehensive test for genetic forms of hearing loss including non-syndromic hearing loss, non-syndromic mimics (such as Usher Syndrome, Deafness-Infertility Syndrome, Perrault Syndrome and Pendred syndrome, among others) and common forms of syndromic hearing loss.

Why genetic testing, why OtoSCOPE® and why the MORL? Simple – get the best.

Methodology: 
Next generation sequencing with read depth analysis for CNV detection.

Turnaround time: 
Turnaround time is approximately 6 weeks.

Sample Required:
8 - 10 cc. whole blood in lavender (EDTA) top tubes OR 10 μg DNA, minimum concentration: 50 ng/μl (A260/A280 1.8-2) resuspended in 0.1mM EDTA (10mM Tris HC1, 0.1mM EDTA, pH 8, Teknova Cat#T0220).

Cost & CPT Codes 
See the MORL Testing Menu

GeneTests GeneReviews - Deafness and Hereditary Hearing Loss Overview