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hearing loss genomic sequencing

Indications: - unexplained hearing loss in infant or child Genetics: - implicated genes: [1] - CDH23 - CLRN1 - GJB2 - GPR98 - MTRNR1 - MYO7A - MYO15A - PCDH15 - OTOF - SLC26A4 - TMC1 - TMPRSS3 - USH1C - USH1G - USH2A - WFS1 [1]

Related

hearing loss (hearing impairment, hard of hearing, HOH)

General

genome sequencing

References

  1. CPT :accession 81430
  2. ARUP Consult: Hearing Loss https://arupconsult.com/ati/Hearing-Loss-Panel