Results 161 to 170 of about 2,830 (205)
Some of the next articles are maybe not open access.

Chorda tympani nerve dysfunction associated with congenital microtia

Acta Oto-Laryngologica, 2017
This 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   +2 more
exaly   +3 more sources

Congenital abnormalities associated with microtia: A 10-YEARS retrospective study

open access: yesInternational Journal of Pediatric Otorhinolaryngology, 2021
International audienceMicrotia is a congenital auricular malformation, often part of a syndromic form (35%-55% of cases). The accurate prevalence of associated malformations remains to be determined with regard to the heterogeneous results of the ...
Sophie Achard   +2 more
exaly   +2 more sources

Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect

open access: yesGenes, 2023
Microtia is a congenital malformation characterized by a small, abnormally shaped auricle (pinna) ranging in severity. Congenital heart defect (CHD) is one of the comorbid anomalies with microtia.
Caiyun Zhu, Bo Pan, Nuo Si
exaly   +2 more sources

Microtia in Indonesia: Characteristics and Family History Analysis on the Presence of Other Congenital Anomalies in Patients With Microtia

Cleft Palate-Craniofacial Journal
Objective This study aims to explore the characteristics of microtia in Indonesia and examine whether family traits influence its severity, focusing on other congenital anomalies in patients categorized as either isolated or syndromic microtia.
Imaniar Fitri Aisyah   +2 more
exaly   +3 more sources

Pathogenic Genes for Congenital Microtia: A Bioinformatics Analysis

Journal of Craniofacial Surgery, 2023
Objective: The purpose of this study is to accurately find the pathogenic genes of congenital microtia, so as to lay a theoretical foundation for genetic screening, diagnosis, and gene therapy of congenital microtia in the further stage.
Pengfei, Sun   +3 more
openaire   +2 more sources

Microtia and Congenital Aural Atresia

Journal of Craniofacial Surgery, 2012
The purpose of this study was to show the clinical characteristics of microtia and congenital aural atresia cases in Turkey and to make the classification. For this purpose, records of 28 patients with microtia who were admitted to the ENT Clinic of Eskisehir Military Hospital, Turkey, between 1995 and 2011 and 3 patients admitted to the ENT outpatient
Selahattin, Genc   +5 more
openaire   +2 more sources

Microtia and Congenital Aural Atresia

Otolaryngologic Clinics of North America, 2007
Microtia and congenital aural atresia (CAA) are congenital anomalies that are so common that every otolaryngologist should be familiar with the initial evaluation and care of the patient. When one ear hears normally, speech and language development should be normal.
Peggy E, Kelley, Melissa A, Scholes
openaire   +2 more sources

Correction of Congenital Microtia Using the Tissue Expander

Plastic and Reconstructive Surgery, 1989
We attempted auricular reconstruction using Radovan-type inflatable silicone expanders in six children and one adult, with the complete hypoplastic, the conchal remnant, and constricted type of microtia. Ear frameworks, including the helix, anthelix, concha, and tragus, were prepared using autologous rib cartilage.
Y, Hata   +4 more
openaire   +3 more sources

The Surgical Repair of Congenital Microtia and Atresia

Otolaryngology–Head and Neck Surgery, 1988
Auricular reconstruction for congenital microtia is a complex multi‐staged procedure. The repair of congenital atresia of the ear is one of the most difficult operations an otologic surgeon may attempt. in order to accomplish both procedures without endangering the integrity of either, there must be proper planning and close cooperation between the ...
E A, Aguilar, R A, Jahrsdoerfer
openaire   +2 more sources

Study on the Incidence of Congenital Genitourinary System Malformations in Congenital Microtia Patients

Journal of Craniofacial Surgery, 2023
Objective: Study the incidence of genitourinary malformations combined with microtia, find the regularity of the disease, and analyze the correlation between them. Methods: There is a total of 3143 microtia patients from January 2015 to December 2019 in Plastic Surgery Hospital.
Dejin, Gao   +3 more
openaire   +2 more sources

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