Anomalies of the auditory organ in trisomy 18 syndrome: human temporal bone histopathological study

Author:

Tadaki Tohru,Kamiyama Ryosuke,Okamura Hiro-Oki,Ohtani Iwao

Abstract

The purpose of this study was to define the histopathological changes in the temporal bone of a fetus with trisomy 18 syndrome, a stillborn due to perosplanchnia. Several anomalies were found including malformation of the auditory ossicles, residual mesenchyme in the middle ear, aberrant tensor tympani muscle, absence of stapedial tendon, aberrant lateral ampullary nerve and wide endolymphatic sinus. The incus body was deformed and separated from the long process by connective tissue and monocrural stapes was noted in the right ear. Three-dimensional reconstruction images provided a clear view of the auditory ossicle malformation. The abnormal findings in our case indicate that ear anomalies in this syndrome might be derived from the component around the first and second branchial arches.

Publisher

Cambridge University Press (CUP)

Subject

Otorhinolaryngology,General Medicine

Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cause, severity, and efficacy of treatment for hearing loss in children with Trisomy 18: A single institution‐based retrospective study;American Journal of Medical Genetics Part A;2023-12-07

2. Evaluation of the stapedial tendon growth dynamic in human fetuses;Surgical and Radiologic Anatomy;2019-04-01

3. Imaging Findings in Syndromes with Temporal Bone Abnormalities;Neuroimaging Clinics of North America;2019-02

4. Trisomy 18 Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

5. Trisomy 18 Syndrome;Atlas of Genetic Diagnosis and Counseling;2016

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