Abnormal Congenital Location of Stapes’ Superstructure: Clinical and Embryological Implications
Congenital middle ear malformations are rare. Most part of them are usually associated with other malformations, such as aural atresia, microtia, and dysmorphic craniofacial features. A clinical case of a 24-year-old male with a right-sided conductive hearing loss since his childhood, without cranio...
Main Authors: | Vânia Henriques, Rafaela Teles, Ana Sousa, Roberto Estevão, Jorge Rodrigues, Alexandra Gomes, Francisco Silva, Ângelo Fernandes, Fausto Fernandes |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2016-01-01
|
Series: | Case Reports in Otolaryngology |
Online Access: | http://dx.doi.org/10.1155/2016/2598962 |
Similar Items
-
Bilateral Congenital Absence of the Stapes Superstructure in Two Siblings
by: Jose Ignacio Undabeitia, et al.
Published: (2014-01-01) -
Anatomopathology of the Superstructure of the Stapes in Patients with Otosclerosis
by: Bettina Carvalho, et al.
Published: (2015-01-01) -
Tympanoplasty with an Intact Stapes Superstructure in Chronic Otitis Media
by: Kurt Schlemmer, et al.
Published: (2021-07-01) -
Two cases of congenital stapes malformation: Implications for development of the stapes footplate and the oval window
by: Hiroki Ishida, et al.
Published: (2020-01-01) -
A Rare Stapes Abnormality
by: Hala Kanona, et al.
Published: (2015-01-01)