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Join us at CI2023

16 January 2023
Registration is now open for CI2023: Cochlear Implants in Children and Adults, 7-10 June, in Dallas, Texas, USA, with early bird rates until 7 April 2023. The conference will explore current and emerging topics for CI patients across the lifespan....

SEQaBOO: SEQuencing a Baby for an Optimal Outcome

1 July 2021 | | Audiology - Adult, Audiology - Diagnostic
There are at least 15 countries now running genome sequencing projects. The team in Manchester, UK, and Boston, USA, share their SEQaBOO project. Abstract SEQaBOO (SEQuencing a Baby for an Optimal Outcome) will transform newborn hearing screening (NBHS) by bringing...
Annals of Otology, Rhinology & Laryngology journal cover image.

Newborn sensorineural hearing loss – what is the incidence?

4 March 2024 | | Audiology - Diagnostic, Auditory Implants, Audiology - Paediatric, Otology, Paediatric ENT | congenital hearing loss, newborn hearing screening, otitis media with effusion, sensorineural hearing loss, vernix
In the last two decades, the introduction of newborn screening for hearing loss has dramatically lowered the average age of newborn hearing loss diagnosis to around two to three months of age. The benefits of early diagnosis are manifold, enabling...

Audiology in this issue... Paediatric Audiology Gamechangers (NovDec18)

7 November 2018
Fifty years ago, the National Conference on Education of the Deaf followed up on the Babbidge Report of 1965, recognising the failure of oralism in deaf education. Because young, deaf children at that time did not have access to sound, they could not develop speech and language. Further, because children were identified at two years or later, early intervention was only a dream.

A snapshot of UK newborn hearing screening services during the COVID-19 pandemic

28 July 2020 | | COVID-19, Audiology - Paediatric, Audiology - Diagnostic
During the COVID-19 pandemic, new guidance for newborn hearing screening programmes and management of audiology referrals was released by Public Health England [1,2]. There was also joint guidance from the UK professional bodies [3] and guidance from NHS England regarding...

Assessment of genetic disorders: congenital sensorineural hearing loss

1 November 2014 | | ENT, Genetics, Otology
Severe or profound sensorineural hearing impairment (SNHI) is a common birth defect, affecting approximately 1 in 1000 newborns [1]. SNHI may result from environmental causes or have a genetic basis. The genetic causes can be further subdivided into non-syndromic (isolated...
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