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1971 1
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International Consensus Recommendations on Microtia, Aural Atresia and Functional Ear Reconstruction.
Zhang TY, Bulstrode N, Chang KW, Cho YS, Frenzel H, Jiang D, Kesser BW, Siegert R, Triglia JM. Zhang TY, et al. J Int Adv Otol. 2019 Aug;15(2):204-208. doi: 10.5152/iao.2019.7383. J Int Adv Otol. 2019. PMID: 31418720 Free PMC article.
Recommendations include the definition and classification of microtia/atresia, treatment of microtia, treatment of congenital aural atresia, flowchart of functional ear reconstruction, and future research directions. Patients with microtia and aural
Recommendations include the definition and classification of microtia/atresia, treatment of microtia, treatment of congenital
Management of Conductive Hearing Loss in Children.
Dougherty W, Kesser BW. Dougherty W, et al. Otolaryngol Clin North Am. 2015 Dec;48(6):955-74. doi: 10.1016/j.otc.2015.06.007. Epub 2015 Sep 8. Otolaryngol Clin North Am. 2015. PMID: 26360369 Review.
Conductive hearing loss (CHL), far more common than sensorineural hearing loss in children, can be acquired or congenital, can range from mild to moderately severe, and can be caused by a simple cerumen impaction, middle ear fluid, or complex middle ear abnormalities with …
Conductive hearing loss (CHL), far more common than sensorineural hearing loss in children, can be acquired or congenital, can range …
Diagnosis and management strategies in congenital atresia of the external auditory canal. Study Group on Otological Malformations and Hearing Impairment.
Declau F, Cremers C, Van de Heyning P. Declau F, et al. Br J Audiol. 1999 Oct;33(5):313-27. doi: 10.3109/03005369909090115. Br J Audiol. 1999. PMID: 10890146 Review.
This consensus report represents a distillation of current opinion regarding diagnosis and management of congenital aural atresia. It also takes into account the philosophical differences which exist in Europe. Congenital aural atresia re …
This consensus report represents a distillation of current opinion regarding diagnosis and management of congenital aural a
Diagnosis and management of salivary fistula after surgery for congenital aural atresia.
Miller RS, Jahrsdoerfer RA, Hashisaki GT, Kesser BW. Miller RS, et al. Otol Neurotol. 2006 Feb;27(2):189-92. doi: 10.1097/01.mao.0000185274.45507.2d. Otol Neurotol. 2006. PMID: 16436988
We present the first described series of patients with salivary fistula after repair of congenital aural atresia. STUDY DESIGN: Retrospective case review from 1985 to 2004. ...RESULTS: Of 1,500 patients operated on for aural atresia, we identifi …
We present the first described series of patients with salivary fistula after repair of congenital aural atresia. STUDY …
Cause, severity, and efficacy of treatment for hearing loss in children with Trisomy 18: A single institution-based retrospective study.
Sato R, Yoshimura H, Kosho T, Takumi Y. Sato R, et al. Am J Med Genet A. 2024 Apr;194(4):e63492. doi: 10.1002/ajmg.a.63492. Epub 2023 Dec 7. Am J Med Genet A. 2024. PMID: 38062644
Trisomy 18 is a common chromosomal aberration syndrome, characterized by variable clinical manifestations, including cardiovascular, pulmonary, genitourinary, and musculoskeletal findings, leading to a shorter survival and severe developmental delay in survivors. However, recentl …
Trisomy 18 is a common chromosomal aberration syndrome, characterized by variable clinical manifestations, including cardiovascular, pulmona …
Congenital aural atresia: anatomy and surgical management.
Nager GT. Nager GT. Birth Defects Orig Artic Ser. 1971 Mar;07(4):33-51. Birth Defects Orig Artic Ser. 1971. PMID: 5173350
A surgical technic for the treatment of Group II (moderately severe) aural atresia is described. Of 21 patients, treated surgically during the past 12 years, 15 patients (71%) gained serviceable hearing. ...
A surgical technic for the treatment of Group II (moderately severe) aural atresia is described. Of 21 patients, treated surgi …
Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.
Feenstra I, Vissers LE, Orsel M, van Kessel AG, Brunner HG, Veltman JA, van Ravenswaaij-Arts CM. Feenstra I, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1858-67. doi: 10.1002/ajmg.a.31850. Am J Med Genet A. 2007. PMID: 17632778
Common clinical features include a characteristic face, short stature, congenital aural atresia (CAA), abnormalities of the feet, and mental retardation (MR). ...
Common clinical features include a characteristic face, short stature, congenital aural atresia (CAA), abnormalities of …