| Literature DB >> 21147207 |
E J J Verver1, K Freriks, H G X M Thomeer, P L M Huygen, R J E Pennings, A A E M Alfen-van der Velden, H J Timmers, B J Otten, C W R J Cremers, H P M Kunst.
Abstract
The aim of the study was to report otologic and audiologic characteristics in a group of children with Turner syndrome (TS) and correlate these findings to karyotype. Additionally, we give recommendations for the otologic care of these children. Sixty children (age 1.7-21.2 years) were included in this retrospective study. Medical history and karyotypes were recorded and otologic and audiologic evaluation was performed. A history of recurrent otitis media was reported in 41/60 (68%) children and 3/60 (5%) had suffered from cholesteatoma. Audiometric data in 56 children revealed that normal hearing was only present in 33/112 (29%) ears. All other ears 79/112 (71%) were classified in five different audiometric categories for hearing loss. Hearing thresholds in general appeared to be about 10-11 dB worse in children with a monosomy 45,X or isochromosome (both have a total deletion of the short (p) arm of the X-chromosome) compared to those having a mosaicism or structural anomaly (partial deletion, or total deletion in only a few cells). Our findings support the hypothesis that hearing can be affected by loss of the p-arm of the X-chromosome. It is for the first time that a relation between hearing problems and karyotype is statistically confirmed in a large group of children with TS.Entities:
Mesh:
Year: 2010 PMID: 21147207 DOI: 10.1016/j.heares.2010.12.007
Source DB: PubMed Journal: Hear Res ISSN: 0378-5955 Impact factor: 3.208