| Literature DB >> 28446373 |
Yoshitaka Takanashi1, Tetsuaki Kawase2, Yasuko Tatewaki3, Jun Suzuki4, Izumi Yahata4, Yuuri Nomura4, Kazuha Oda4, Hiromitsu Miyazaki4, Yukio Katori4.
Abstract
Internal auditory canal anomalies are rare. Narrow internal auditory canal is believed to occur as a result of aplasia or hypoplasia of the vestibulocochlear nerve. Narrow duplication of the internal auditory canal is considered to be very rare. Narrow duplication of the internal auditory canal with inner ear malformation has been reported in only 3 cases. We present 2 cases of narrow duplication of the internal auditory canal with inner ear malformation. The first case had inner ear malformation on only one side and the second case had inner ear malformation on both sides. The embryogenesis may be different between internal auditory canal and inner ear.Entities:
Keywords: 3D-CT; Duplicated IAC; Inner ear malformation
Mesh:
Year: 2017 PMID: 28446373 DOI: 10.1016/j.anl.2017.03.019
Source DB: PubMed Journal: Auris Nasus Larynx ISSN: 0385-8146 Impact factor: 1.863