TY - JOUR T1 - A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort JF - BMJ Paediatrics Open DO - 10.1136/bmjpo-2017-000119 VL - 1 IS - 1 SP - e000119 AU - Lilian Downie AU - Jane L Halliday AU - Rachel A Burt AU - Sebastian Lunke AU - Elly Lynch AU - Melissa Martyn AU - Zeffie Poulakis AU - Clara Gaff AU - Valerie Sung AU - Melissa Wake AU - Matthew Hunter AU - Kerryn Saunders AU - Elizabeth Rose AU - Heidi L Rehm AU - David J Amor Y1 - 2017/09/01 UR - http://bmjpaedsopen.bmj.com/content/1/1/e000119.abstract N2 - Introduction The aetiology of congenital hearing loss is heterogeneous, and in many infants a genetic cause is suspected. Parents face a diagnostic odyssey when searching for a cause of their infant’s hearing loss. Through the Melbourne Genomics Health Alliance, a prospective cohort of infants will be offered whole-exome sequencing (WES) with targeted analysis in conjunction with chromosome microarray to determine the genetic causes of congenital hearing loss. Parents will also be offered the opportunity to receive additional results from their infant’s WES.Methods Eligible infants will be identified through the Victorian Infant Hearing Screening Program and offered an appointment in a paediatrician-run clinic, a genetics assessment and enrolment in the Victorian Childhood Hearing Impairment Longitudinal Databank. If parents consent to WES, genes causing deafness will be analysed and they can choose to obtain additional findings. For the additional results component, a modified laboratory protocol has been designed for reporting of results in the absence of a relevant phenotype. Parents’ experience of being offered WES will be evaluated using surveys.Discussion This project will provide descriptive analysis of the genetic aetiology of congenital hearing loss in this cohort and may provide data on genotype–phenotype correlations. Additionally, choices regarding additional findings will be analysed. Participants will represent a diverse cross section of the population, increasing the ability to generalise results beyond the study group. Evaluation surveys will allow analysis of preferences around counselling, usefulness of a decision aid and adequacy of information provision. ER -