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Tragus formation during concha-type microtia repair using a chondrocutaneous island flap

Ha JH, Jeong E, Lazaro H

Formation of an ideally-shaped tragus remains one of the most challenging issues during staged tragus reconstruction in microtia patients. The authors describe a new method used to treat a unique...
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Ectopic Preauricular Sinus in a Facial Cleft and Microtia Patient

Park JY, Lee S, Kim HJ, Jung SG

Preauricular sinus is a congenital malformation that is very commonly encountered among the general population and it has especially high prevalence among Asians when compared to other ethnic groups. It...
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Analysis of Inner Ear Anomalies in Unilateral Congenital Aural Atresia Combined With Microtia

Park E, Lee G, Jung HH, Im GJ

OBJECTIVES: The aim of this study was to analyze the incidence of inner ear anomalies in patients with unilateral congenital aural atresia (CAA) combined with microtia. METHODS: We retrospectively reviewed 61...
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Reconstruction of Congenital Aural Malformation

Oh JH

The complexity of the auricle makes its reconstruction technically difficult, owing to the convexities and concavities of the underlying cartilage with its tightly adherent and thin overlying skin. This article...
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Anatomical variants of the superficial temporal artery in patients with microtia: a pilot descriptive study

Imran FH, Yong CK, Das S, Huei YL

Superficial temporal artery (STA) based pedicled fascial flap plays a pivotal role in ear reconstruction for microtia patients. There is paucity of literature on the anatomy of the STA in...
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Safety and efficacy of transcutaneous bone conduction implant surgery for hearing improvement in microtia patients with bilateral hearing impairment

Cheon JH, Lee HC, Im GJ, Park JY, Park C

BACKGROUND: In microtia patients with bilateral hearing impairment, hearing improvement is crucial for language development and performance. External auditory canal reconstruction (EACR) has been performed to improve hearing, but often...
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Chromosome 11q13 deletion syndrome

Kim YS, Kim GH, Byeon JH, Eun SH, Eun BL

Chromosome 11q13 deletion syndrome has been previously reported as either otodental syndrome or oculo-oto-dental syndrome. The otodental syndrome is characterized by dental abnormalities and high-frequency sensorineural hearing loss, and by...
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