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SHORT REPORT Audiological profile in Apert syndrome (1970)
https://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.660.9062#:~:text=A%20pert%20syndrome%20is%20a%20rare%20easily%20identifiable,loss%20is%20known%20to%20occur%20in%20Apert%20syndrome.
Audiological profile in Apert syndrome - PubMed
https://pubmed.ncbi.nlm.nih.gov/15908623/
Apert syndrome is one of the craniosynostosis syndromes and is commonly associated with conductive hearing loss, but there are contradicting reports regarding the cause. Retrospective analysis of case notes of Apert syndrome patients seen between 1970 and 2003 was therefore undertaken. Seventy case notes were obtained; 59% were males.
Audiological profile in Apert syndrome | Archives of ...
https://adc.bmj.com/content/90/6/592
Abstract. Apert syndrome is one of the craniosynostosis syndromes and is commonly associated with conductive hearing loss, but there are contradicting reports regarding the cause. Retrospective analysis of case notes of Apert syndrome patients seen between 1970 and 2003 was therefore undertaken. Seventy case notes were obtained; 59% were males.
(PDF) Audiological profile in Apert syndrome
https://www.researchgate.net/publication/7832261_Audiological_profile_in_Apert_syndrome
We found mild or moderate hearing loss in 44.0% of patients with Apert syndrome, in 28.5% with Crouzon syndrome, in 62.1% with Muenke syndrome, …
SHORT REPORT Audiological profile in Apert syndrome
https://ern-ithaca.eu/wp-content/uploads/2020/12/Rajenderkumar_Apert_Hearing_ArchDisChild2005.pdf
Audiological profile in Apert syndrome D Rajenderkumar, D-E Bamiou, T Sirimanna..... Arch Dis Child 2005;90:592–593. doi: 10.1136/adc.2004.067298 Apert syndrome is one of the craniosynostosis syndromes and is commonly associated with conductive hearing loss, but there are contradicting reports regarding the cause.
SHORT REPORT Audiological profile in Apert syndrome …
https://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.660.9062
A pert syndrome is a rare easily identifiable syndromic type of craniosynostosis characterised by midfacial malfor-mations and syndactyly of the hands and feet, which minimally involves digits 2, 3, and 4.1 It has a birth prevalence estimated to be between 9.9/million and 15.5/million and accounts for about 4.5 % of all cases of craniosynostosis.2 3 Hearing loss is known to occur in …
Audiological profile of children and young adults with ...
https://www.ncbi.nlm.nih.gov/pubmed/21844411
RESULTS: We found mild or moderate hearing loss in 44.0% of patients with Apert syndrome, in 28.5% with Crouzon syndrome, in 62.1% with Muenke syndrome, in 28.6% with Saethre-Chotzen syndrome, and in 6.7% with complex craniosynostosis.
Audiological Profile of Children and Young Adults With ...
https://jamanetwork.com/journals/jamaotolaryngology/fullarticle/1106416
Results We found mild or moderate hearing loss in 44.0% of patients with Apert syndrome, in 28.5% with Crouzon syndrome, in 62.1% with Muenke syndrome, in 28.6% with Saethre-Chotzen syndrome, and in 6.7% with complex craniosynostosis. Hearing loss was conductive in most patients with Apert, Crouzon, and Saethre-Chotzen syndromes and it was …
Vestibular dysfunction in Apert Syndrome Hearing, …
https://www.rareconnect.org/uploads/documents/vestibular-dysfunction-in-apert-syndrome.pdf
loss in 70 Apert syndrome patients. They concluded that otitis media with effusion was the main cause of hearing impairment, with a 3 – 6% incidence of con-genital hearing impairment observed (4,9). Although the audiological aspects of Apert syn-drome are well documented, there is limited infor-mation and evidence regarding structural inner ear
Treatment timing and multidisciplinary approach in Apert ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525098/
Conductive hearing loss is common in Apert syndrome. This results from chronic otitis media and occasionally from middle ear anomalies (9). The ears are set low and may be enlarged. Bilateral symmetrical complex syndactyly of …
Audiological profile in Apert syndrome - CORE
https://core.ac.uk/display/208619055
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