Results 131 to 140 of about 2,486 (175)
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Management of Congenital Aural Atresia and Microtia
Otolaryngology–Head and Neck Surgery, 1995Educational objectives: To evaluate and properly diagnose anatomic deformities of the auricle and to properly treat these problems.
Robert O. Ruder +2 more
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Epidemiological Research of Microtia Combined With Congenital Heart Disease
Journal of Craniofacial Surgery, 2020Summary: Congenital heart disease (CHD) is one of the most common combined malformations of microtia. There is currently no specific study that investigates the relationship between microtia and CHD. Methods: This study collected microtia inpatients admitted from May 1, 2015 to July
Tongyu, Cao +5 more
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Auricular Reconstruction of Congenital Microtia (Grade III)
The Laryngoscope, 1996AbstractThe auricular deformity of congenital microtia (Grade III) is almost always associated with congenital atresia, an affliction that can cause devastating physical and psychological trauma in children. Auricular reconstruction for congenital microtia (Grade III) should provide a child with a reasonable facsimile of an ear through a limited number
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Congenital Microtia: Reconstruction With a Silicone Rubber (Silastic) Prosthesis
Archives of Otolaryngology - Head and Neck Surgery, 1971The artistic surgical anatomy of the external ear is delicate and difficult to duplicate. The Cronin Silicone rubber (Silastic) otoplasty prosthesis for subcutaneous implantation allows a good cosmetic result in two stages. A not infrequent complication is exposure of the silicone rubber frame.
J O, Stallings +4 more
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Combined reconstruction of congenital auricular atresia and severe microtia
The Laryngoscope, 2003AbstractObjectives: Due to their embryologic developments, auricular atresia and severe microtia are in most cases combined malformations. The aims of this study were to develop a surgical technique for combined esthetic and functional reconstruction with a minimum of operations and to evaluate the results. Study Design: Prospective clinical evaluation.
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Pedigree and Genetic Study of a Bilateral Congenital Microtia Family
Plastic and Reconstructive Surgery, 2010Microtia can be defined as a malformation of the auricle; the varying severity that results can range from mild distortion of the anatomic landmarks to the complete absence of the ear. No specific study has been reported analyzing a family of several generations with bilateral congenital concha-type microtia so far.The authors obtained medical records ...
Qingguo, Zhang, Jiao, Zhang, Wei, Yin
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Chorda tympani nerve dysfunction associated with congenital microtia
Acta Oto-Laryngologica, 2017This is the first report to investigate the correlation between ear anomalies related to the development of specific ear structures and chorda tympani dysfunction (CTD) in congenital microtia. CTD is not always consistent with the severity of the ear anomaly or the presence of facial nerve paralysis (FNP).To investigate the relationship between the ...
Kenichi, Takano +4 more
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Microtia and Other Congenital Auricular Deformities
2017Ear deformities have been classified as a continuum ranging from anotia to prominent ear. Microtia literally means small ear, and it presents a congenitally small and malformed external ear. The incidence of microtia is 1 in 7000–8000 live births, and it is unilateral in 80–90% of cases.
Aleksandar M. Vlahovic, Emir Q. Haxhija
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Modification in the Technique of Ear Framework Fabrication for Congenital Microtia
Journal of Craniofacial Surgery, 2012Ear framework fabrication with autologous costal cartilage is considered to be one of the important factors for successful auricular reconstruction. Congenital microtia in adults has many particular physiological characteristics different from that in children.
Xu, Zhou +8 more
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Congenital Microtia and Meatal Atresia: Observations and Aspects of Treatment
Archives of Otolaryngology - Head and Neck Surgery, 1957Material, Sex, Side Affected The material consists of microtias and meatal atresias found in patients admitted to the University Oto-Laryngological Hospital at Helsinki from the beginning of the year 1951 to the end of February, 1957. The total number of patients observed and treated was 74, males numbering 50 and females 24.
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