Document Detail


Audiologic findings in saethre-chotzen syndrome.
MedLine Citation:
PMID:  21532428     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
BACKGROUND: : Hearing loss has been described in Apert syndrome but is poorly documented in other craniosynostosis disorders.
METHODS: : The authors retrospectively reviewed the audiologic and otologic records of patients with Saethre-Chotzen syndrome to define the incidence, type, and extent of hearing loss. Only patients with documented audiologic examinations were included. Hearing loss was categorized by American Speech-Language-Hearing Association guidelines (i.e., mild, 26 to 40 dB; moderate, 41 to 55 dB; moderate/severe, 56 to 70 dB; severe, 71 to 90 dB; and profound, >90 dB).
RESULTS: : Twenty-nine patients met inclusion criteria. Mean age at initial audiologic evaluation was 6.7 years (range, 0.7 to 24.5 years). Seventeen patients (59 percent) had at least one abnormal audiogram; in 15 patients, the deficit was mild. Eight patients demonstrated sensorineural hearing loss. Five cases resolved and, thus, had been mischaracterized. Six patients had conductive hearing loss on at least one examination; follow-up testing in four patients revealed normal hearing. Two patients had unspecified hearing loss by sound field method. One patient had mixed hearing loss on consecutive audiograms. Twenty-one patients (72 percent) had normal hearing on their last audiogram.
CONCLUSIONS: : Most patients with Saethre-Chotzen syndrome had hearing loss at some point during childhood. This was typically mild and correlated with middle ear abnormality and eustachian tube dysfunction. Usually, the hearing deficit resolved. Early mischaracterization of mixed hearing loss or conductive hearing loss as sensorineural hearing loss was common.
Authors:
Heather Rosen; Brian T Andrews; John G Meara; Joan M Stoler; John B Mulliken; Gary F Rogers
Related Documents :
10808678 - Bone mineral density in primary and secondary amenorrhea.
50628 - Solitary myeloma. a study of 10 black patients during an 8-year period.
10847438 - Decreased trabecular bone mineral density in newly diagnosed inflammatory bowel disease...
21325348 - Anaemia and resistance to erythropoiesis-stimulating agents as prognostic factors in ha...
18617438 - Independence of restrictive filling pattern and lv ejection fraction with mortality in ...
10840088 - Evaluation of male sexual function after pelvic trauma by the international index of er...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Plastic and reconstructive surgery     Volume:  127     ISSN:  1529-4242     ISO Abbreviation:  Plast. Reconstr. Surg.     Publication Date:  2011 May 
Date Detail:
Created Date:  2011-05-02     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  1306050     Medline TA:  Plast Reconstr Surg     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2014-20     Citation Subset:  AIM; IM    
Affiliation:
Boston, Mass. From the Departments of Plastic and Oral Surgery and Genetics, Children's Hospital Boston.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Distraction osteogenesis of costocartilaginous rib grafts and treatment algorithm for severely hypop...
Next Document:  Alloplastic augmentation of the facial skeleton: an occasional adjunct or alternative to orthognathi...