Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/17469
Title: A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort.
Authors: Downie, Lilian;Halliday, Jane L;Burt, Rachel A;Lunke, Sebastian;Lynch, Elly;Martyn, Melissa;Poulakis, Zeffie;Gaff, Clara;Sung, Valerie;Wake, Melissa;Hunter, Matthew;Saunders, Kerryn;Rose, Elizabeth;Rehm, Heidi L;Amor, David J
Affiliation: Victorian Clinical Genetics Services, Victoria, Melbourne, Australia
Murdoch Children's Research Institute, Victoria, Melbourne, Australia
Royal Children's Hospital, Victoria, Melbourne, Australia
Department of Paediatrics, University of Melbourne, Victoria, Melbourne, Australia
Melbourne Genomics Health Alliance, Victoria, Melbourne, Australia
Austin Health, Heidelberg, Victoria, Australia
University of Auckland, Auckland, New Zealand
Monash Health, Victoria, Melbourne, Australia
Monash University, Victoria, Melbourne, Australia
Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA
Issue Date: 2017
EDate: 2017-09-14
Citation: BMJ paediatrics open 2017; 1(1): e000119
Abstract: 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. 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. 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.
URI: http://ahro.austin.org.au/austinjspui/handle/1/17469
DOI: 10.1136/bmjpo-2017-000119
ORCID: 0000-0003-3914-5592
PubMed URL: 29637142
Type: Journal Article
Subjects: Deafness
Genetics
Screening
Appears in Collections:Journal articles

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