Sensorineural hearing loss and hypoplastic cochlea in Axenfeld-Rieger syndrome with FOXC1 mutation. Issue 6 (December 2021)
- Record Type:
- Journal Article
- Title:
- Sensorineural hearing loss and hypoplastic cochlea in Axenfeld-Rieger syndrome with FOXC1 mutation. Issue 6 (December 2021)
- Main Title:
- Sensorineural hearing loss and hypoplastic cochlea in Axenfeld-Rieger syndrome with FOXC1 mutation
- Authors:
- Yamazaki, Hiroshi
Nakamura, Takeshi
Hosono, Katsuhiro
Yamaguchi, Tomoya
Hiratsuka, Yasuyuki
Hotta, Yoshihiro
Takahashi, Makio - Abstract:
- Abstract: Objective: Axenfeld-Rieger syndrome (ARS) type 3 is a rare autosomal dominant disease, characterized by anterior segment dysgenesis of the eye, hearing loss, and cardiac defects. ARS type 3 is highly associated with FOXC1 mutations, which induces developmental disorders of neural crest cells. Most studies about ARS patients focused on ophthalmologic findings, but details in their hearing loss have not yet been revealed. In this report, we investigated audiological and otological manifestations in the ARS type 3 patient who had the novel heterozygous FOXC1 mutation leading deletion at the forkhead DNA-binding domain. Methods and Results: Pure tone audiometry showed bilateral sensorineural hearing loss (SNHL) and audiological examinations confirmed that major dysfunctions existed in the cochlea, rather than the spiral ganglion neurons and the cochlear nerve. CT and MRI revealed the hypoplastic cochlea at both sides. Given that the 6p25 deletion syndrome, lacking one allele of the FOXC1 gene, shows similar, but more severe cochlear malformations than the present case, the FOXC1 mutations might contribute to the hypoplasia and dysfunctions in the cochlea. Conclusion: To our knowledge, this is the first report demonstrating that the ARS type 3 patient with the FOXC1 mutation has the hypoplasia and dysfunctions in the cochlea, which results in bilateral SNHL.
- Is Part Of:
- Auris nasus larynx. Volume 48:Issue 6(2021)
- Journal:
- Auris nasus larynx
- Issue:
- Volume 48:Issue 6(2021)
- Issue Display:
- Volume 48, Issue 6 (2021)
- Year:
- 2021
- Volume:
- 48
- Issue:
- 6
- Issue Sort Value:
- 2021-0048-0006-0000
- Page Start:
- 1204
- Page End:
- 1208
- Publication Date:
- 2021-12
- Subjects:
- Axenfeld-Rieger syndrome -- Sensorineural hearing loss -- FOXC1 -- Malformation -- Inner ear
Otolaryngology -- Periodicals
Electronic journals
616 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03858146 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03858146 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03858146 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.anl.2020.07.006 ↗
- Languages:
- English
- ISSNs:
- 0385-8146
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1792.760000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18474.xml