Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis. Issue 1 (21st March 2021)
- Record Type:
- Journal Article
- Title:
- Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis. Issue 1 (21st March 2021)
- Main Title:
- Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis
- Authors:
- Chen, Anhai
Song, Jian
Acke, Frederic R. E.
Mei, Lingyun
Cai, Xinzhang
Feng, Yong
He, Chufeng - Abstract:
- Abstract: Branchiootorenal spectrum disorder (BORSD) is a group of rare autosomal dominant entities characterized by branchiogenic malformations, hearing loss (HL) and renal anomalies. It comprises branchiootorenal syndrome and branchiootic syndrome, distinguished by the presence or absence of renal abnormalities. Pathogenic variants have been discovered in the following genes: EYA1, SIX5, SIX1 and SALL1 . As the otological phenotype in BORSD is inconsistently reported, we performed a systematic review to provide an up‐to‐date overview, correlated with the genotype. Forty publications were included, describing 295 individual patients. HL was diagnosed in 95%, usually bilateral and mixed‐type, and differed among the different genes involved. Mixed moderate‐to‐severe HL was the predominant finding in patients with EYA1 involvement, regardless of the presence of renal abnormalities. The sensorineural HL of profound severity was more prevalent in patients with SIX1 mutations. No significant differences among different mutation types or location within the genes could be observed. Structural otological manifestations, ranging from periauricular to inner ear anomalies, were common in both genes. Especially periauricular anomalies were more common and more severe in EYA1 . In summary, otological differences among the different genes involved in BORSD are observed, so the molecular analysis is strongly advised. Abstract :
- Is Part Of:
- Clinical genetics. Volume 100:Issue 1(2021)
- Journal:
- Clinical genetics
- Issue:
- Volume 100:Issue 1(2021)
- Issue Display:
- Volume 100, Issue 1 (2021)
- Year:
- 2021
- Volume:
- 100
- Issue:
- 1
- Issue Sort Value:
- 2021-0100-0001-0000
- Page Start:
- 3
- Page End:
- 13
- Publication Date:
- 2021-03-21
- Subjects:
- branchial‐oto‐renal syndrome -- branchio‐otic syndrome -- branchiootorenal spectrum disorder -- genotype -- hearing loss -- phenotype
Medical genetics -- Periodicals
616.0420 - Journal URLs:
- http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cge.13949 ↗
- Languages:
- English
- ISSNs:
- 0009-9163
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17525.xml