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Home > Laboratory for Molecular Medicine > Tests > Hearing Loss

LMM Tests

  • Cardiomyopathy
    • Pan Cardiomyopathy
    • Transthyretin Amyloidosis
  • Genome Services
    • Diagnostic Exome Sequencing
    • Diagnostic Genome Sequencing
    • Genomic Screening
  • Hearing Loss
    • Connexin Test
    • OtoGenome Panel (110 Genes)
    • Comprehensive DFNB1 and STRC Panel
    • Comprehensive STRC / Deafness and Male Infertility Syndrome Test
    • SLC26A4 Gene Sequencing
    • WFS1 Gene Sequencing
    • POU3F4 Gene Sequencing
  • Kidney Disease
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Hearing Loss Tests

The Laboratory for Molecular Medicine at Partners HealthCare Personalized Medicine offers genetic testing for syndromic and nonsyndromic forms of hearing loss.

Otogenome Test

  • OtoGenome™ Test for Hearing Loss and Related Syndromes (110 Genes)* 

Common Autosomal Recessive Hearing Loss Tests

  • Comprehensive DFNB1 and STRC Panel 
  • Connexin Test: GJB2 Sequencing and DFNB1 (GJB6) Deletion
  • Comprehensive STRC / Deafness and Male Infertility Syndrome Test

Pendred Syndrome or Hearing Loss with EVA

  • SLC26A4 (PDS) Gene Test

Low-frequency NonSyndromic Hearing Loss

  • WFS1 Gene Sequencing Test

X-linked Hearing Loss with Stapes Fixation or Perilymphatic Gusher

  • POU3F4 Gene Test

* Single gene testing is available for some genes included in the OtoGenome™ Test . Please inquire for more information.

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