Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel
| Test Information | |
|---|---|
| Test Name | Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel |
| Lab (Location) | The Hospital for Sick Children |
| Category | Audiology |
| Subcategory | Common and Non-Syndromic Hearing Loss |
| Gene/Platform/Region List | ACTG1, ADGRV1, CDH23, CHD7, CLDN14, COCH, DFNA5, DFNB59, DIAPH1, ESPN, ESRRB, EYA1, EYA4, GIPC3, GJB2, GJB6, GPSM2, GRHL2, GRXCR1, HGF, ILDR1, KCNE1, KCNQ1, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, OTOG, OTOGL, PCDH15, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, SERPINB6, SIX1, SLC17A8, SLC26A4, SMPX, STRC, TECTA, TMC1, TMIE, TMPRSS3, TPRN, TRIOBP, USH2A, WFS1 |
| Test type | Gene Panel |
| Samples Accepted | Blood, DNA, DNA (Not Accepted for MLPA) |
| Indications Diagnosis | Diagnosis, Prenatal |
| Test Methodology | CNV, Sequencing |
| Methodology Notes | Exome; MLPA: STRC dosage |
| Diseases/Conditions | Common and Non-Syndromic Hearing Loss |
| Notes | DNA not accepted for MLPA |