Development of in‐house genetic screening for pediatric hearing loss

Objectives To evaluate the efficiency of in‐house genetic testing for mutations causing the most common types of inherited, nonsyndromic, sensorineural hearing loss (SNHL). Methods Retrospective cohort study of 200 patients at a single, pediatric medical center with suspected or confirmed hearing lo...

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Veröffentlicht in:Laryngoscope investigative otolaryngology 2020-06, Vol.5 (3), p.497-505
Hauptverfasser: Doerfer, Karl W., Sander, Tara, Konduri, Girija G., Friedland, David R., Kerschner, Joseph E., Runge, Christina L.
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Sprache:eng
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Zusammenfassung:Objectives To evaluate the efficiency of in‐house genetic testing for mutations causing the most common types of inherited, nonsyndromic, sensorineural hearing loss (SNHL). Methods Retrospective cohort study of 200 patients at a single, pediatric medical center with suspected or confirmed hearing loss who underwent either send out vs in‐house genetic testing for mutations in GJB2/GJB6, SLC26A4, and MTRNR1. Primary outcome measure was the difference in mean turnaround time for send‐out vs in‐house genetic testing. Additional outcomes included associations between audiometric findings and genetic test results. Results One hundred four send‐out tests were performed between October 2010 and June 2014, and 100 in‐house tests were performed between November 2014 and November 2016. The mean turnaround time for send‐out testing was 53.7 days. The mean turnaround time for in‐house testing was 18.9 days. This difference was statistically significant (P 
ISSN:2378-8038
2378-8038
DOI:10.1002/lio2.379