Unspecified Hearing Loss

Tests Available

Forms and Documents

Test Details

ADGRV1 (GPR98), CDH23, CLRN1, DFNB31 (WHRN), MYO7A, PCDH15, PDZD7, USH1C, USH1G, USH2A
  • Congenital deafness and/or moderate to severe hearing loss
  • Problems with balance
  • Decreased night vision
  • Retinitis pigmentosa
  • Next-Gen Sequencing
  • Exon Array Dx

Ordering

T006
4 weeks
2-5 mL Blood - Lavender Top Tube
Buccal Swab

Billing

81404x2; 81407x1; 81408x2
No
Yes
* For price inquiries please email zebras@genedx.com

References

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  2. Yan et al., (2010) J Hum Genet 55:327-335 (PMID: 20379205)
  3. Millan et al., (2011) J Ophthalmol Volume 2011:1-8 (PMID: 21234346)
  4. Adato et al., (2002) Eur J Hum Genet 10:339-350 (PMID: 12080385)
  5. Bitner-Glindzicz et al., (2000) Nat Genet 26:56-60 (PMID: 10973248)
  6. Roux et al., (2006) J Med Genet 43:763-768 (PMID: 16679490)
  7. Adato et al., (1997) Am J Hum Genet 61:813-821 (PMID: 9382091)
  8. Hilgert et al., (2009) J Hum Med Genet 46:272-276 (PMID: 19357116)
  9. Bennett et al., (2004) Pharmacogenomics 5:433-8 (PMID: 15165179)
  10. Pieke Dahl et al., (1996 ) J Med Genet 33:753-7 (PMID: 8880575)
  11. Weston et al., 2000 Am J Hum Genet 66:1199-210 (PMID: 10729113)
  12. van Wijk et al., (2004) Am J Hum Genet 74:738-744 (PMID: 15015129)
  13. Aller et al., (2010) Invest Ophthalmol and Vis Sci 51(11):5480-5485 (PMID: 20538994)
  14. Roux et al., (2011) Invest Ophthalmol Vis Sci. 8;52(7):4063-71 (PMID: 21436283)
  15. Besnard et al., (2012) Hum Mutat 33(3):504-10 (PMID: 22147658)
  16. Ebermann et al., (2010) The Journal of Clinical Investigation 120(6):1812-23 (PMID: 20440071)