Audiological abnormalities in the Klippel-Feil syndrome
a Department
of Clinical Genetics, St Mary's Hospital, Manchester, UK, b Hearing Assessment Centre, Timperley Health Centre,
Trafford Health Care NHS Trust, Timperley, UK, c University Department of Audiological Medicine, Manchester
Royal Infirmary, Manchester, UK
Correspondence to: Dr McGaughran, Department of Clinical Genetics, St Mary's Hospital, Hathersage Road, Manchester M13 0JH, UK.
Accepted 28 April 1998
Klippel-Feil syndrome (KFS) is defined as a short neck with
decreased movement and low posterior hairline. Radiologically, there is
a failure of cervical segmentation. Deafness is a well known associated
feature and may be of sensorineural, conductive, or mixed type. The
audiological assessment of 44 patients with KFS is reported. Thirty
five were found to have abnormalities on audiological testing. The
presence of other features in these patients, reviews of data from
other reports, and the need for further study are discussed.
© 1998 by Archives of Disease in Childhood
This article has been cited by other articles:
-
Alasti, F, Van Camp, G
(2009). Genetics of microtia and associated syndromes. J. Med. Genet.
46: 361-369
[Abstract] [Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.



