Results 61 to 70 of about 4,707 (196)

Otologic and Audiology Concerns of Microtia Repair

, 2017
Microtia is a congenital auricular deformity that commonly presents with associated congenital aural atresia. The most acute concern in these patients is concomitant hearing loss at birth.
Kriti Mohan, Kausar Ali, Yi-Chun Liu
core   +1 more source

Occurrence of Different External Ear Deformities in Monozygotic Twins: Report of 2 Cases

Plastic and Reconstructive Surgery, Global Open, 2014
Summary: Microtia is a spectrum of congenital deformities, which varies from barely discernable to anotia. Twinning is a well-known risk factor for congenital defects including external ear deformities.
Jin-Tian Hu, MD, Tun Liu, MD, Jin Qian, MD, Yong-Biao Zhang, PhD, Xu Zhou, MD, Qing-Guo Zhang, MD   +5 more
doaj   +1 more source

Current Evidence of the Effect of Breastfeeding on Ear Molding Outcomes: A Scoping Review

The Laryngoscope, Volume 136, Issue 7, Page 2868-2875, July 2026.
ABSTRACT Objective To provide an overview on auricular molding and to investigate whether breastfeeding is associated with greater cartilage malleability or improved perinatal auricular molding outcomes. Data Sources Embase, MEDLINE, and CENTRAL databases.
Harry Chiang, Samuel R. Shing, Peggy Su‐Genyk, Lilun Li, Kelvin Kwong, Joseph B. Vella   +5 more
wiley   +1 more source

Non-syndromic Microtia/CAA Scoping Review

, 2023
Scoping review of genetics and pattern of inheritance for microtia and congenital aural ...
David W. Chou, Aparna Govindan, Mingyang Gray, Carly Fiest, Maura Cosetti, Mia Saade   +5 more
core   +1 more source

A Case Report of Congenital Microtia-Atresia

Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, 2021
Background and Objectives: Microtia-atresia is a rare congenital anomaly, which characterized by a small, abnormally shaped auricle (microtia) accompanied with narrow, blocked or absent ear canal (atresia). Microtia can occur appear either as independent
Marzieh Alipour, Khalil Khashei
doaj  

From Expectations to Experience: A Comparison of Program Director Priorities to Resident Case Logs

The Laryngoscope, Volume 136, Issue 7, Page 2954-2962, July 2026.
The present study identified 47 essential otolaryngology procedures via program director surveys and evaluated the extent of resident participation in these cases through ACGME case logs. Results revealed significant variability in surgical experience, with nearly half of these essential procedures being logged fewer than 10 times during residency ...
Taylor S. Erickson, Yoon Soo Park, Sean Hogan, Sophie Yu, Steven D. Pletcher, Sonya Malekzadeh, Stacey T. Gray, Jenny X. Chen   +7 more
wiley   +1 more source

Clinical and radiological evaluation in children with microtia

, 1999
The management of a child with congenital ear malformation, in particular if the external ear is severely involved, is difficult because of the complexity of the therapeutic problem, and that of parental anxiety.
GARANI, Giampaolo, MARTINI, Alessandro, CALZOLARI, Ferdinando, SENSI, Alberto   +3 more
core   +2 more sources

Multi-omics analysis of a case of congenital microtia reveals aldob and oxidative stress associated with microtia etiology

Orphanet Journal of Rare Diseases
Background Microtia is reported to be one of the most common congenital craniofacial malformations. Due to the complex etiology and the ethical barrier of embryonic study, the precise mechanisms of microtia remain unclear.
Wenbo Liu, Yi Wu, Rulan Ma, Xinxi Zhu, Rui Wang, Lin He, Maoguo Shu   +6 more
doaj   +1 more source

The role for cochlear implants in microtia and congenital aural atresia: A case report and a review of literature

Proceedings of Singapore Healthcare, 2023
Sensorineural hearing loss resulting from microtia and aural atresia is rare due to different embryologic origins of the external and inner ear. Consequently, cochlear implants are seldom performed in patients with microtia and/or aural atresia.
Wei Li Neo, Barrie Yau Boon Tan, Adam Ping Meng Tan, Olivia May Ling Wee, Jiun Fong Thong   +4 more
doaj   +1 more source

Prenatal Diagnosis of a Fetus With Congenital Malformations Caused by Compound Heterozygous Mutations in FANCA: A Case Report and Literature Review

Molecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.
This study identified novel compound heterozygous mutations in the FANCA gene that underlie fetal limb‐kidney malformations. Through systematic reviews, we explore the relationship between FANC genotypes and malformation phenotypes, emphasizing the importance of considering Fanconi anemia in the prenatal diagnosis of structural abnormalities to ...
Zedong Yang, Yuchen Ma, Ju Wang, Jiangbo Qu, Shihua Cui, Dongyi Yu   +5 more
wiley   +1 more source