Hearing Loss Gene Tests

NONSYNDROMIC HEARING LOSS

• Connexin Test (GJB2 Sequencing and GJB6-D13S1830 Deletion)
• OtoGenome Test for Hearing Loss (71 Genes)*
• Mitochondrial Gene Panel (MTRNR1 and MTTS1)
  

PENDRED SYNDROME or HEARING LOSS with EVA

• SLC26A4 (PDS) Gene Test

USHER SYNDROME

• Usher Syndrome Panel (9 Genes)* 

BRANCHIO-OTO-RENAL SYNDROME (BOR)

• EYA1 Gene Sequencing Test
• EYA1 Deletion/Duplication Test

AUDITORY NEUROPATHY/DYS-SYNCHRONY

• Auditory Neuropathy Panel (OTOF and DFNB59)

LOW FREQUENCY NONSYNDROMIC HEARING LOSS

• WFS1 Gene Sequencing Test

X-LINKED HEARING LOSS

• POU3F4 Gene Test

ETHNICITY BASED TESTING

• Ashkenazi Jewish Panel for Hearing Loss and Usher (35delG & 167delT in GJB2, GJB6-D13S1830 deletion, Arg245X in PCDH15, Asn48Lys in CLRN1)
• Acadian/French Canadian Usher Panel (216G>A in USH1C and 4338_4339delCT in USH2A)
  
• Finnish Common Mutation for Usher Syndrome (Tyr176X in CLRN1)

* Individual Genes: Some genes included in the OtoGenome and Usher Syndrome Panel have individual testing available. Please inquire for more information.