A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G > T variant
Tekijät: Bharadwaj Thashi, Schrauwen Isabelle, Acharya Anushree, Nouel-Saied Liz M., Väisänen Marja-Leena, Kraatari Minna, Rahikkala Elisa, Jarvela Irma, Kotimäki Jouko, Leal Suzanne M.
Kustantaja: WILEY
Julkaisuvuosi: 2022
Journal: Molecular Genetics and Genomic Medicine
Lehden akronyymi: MOL GENET GENOM MED
Artikkelin numero: e1866
Vuosikerta: 10
Numero: 3
Sivujen määrä: 5
ISSN: 2324-9269
eISSN: 2324-9269
DOI: https://doi.org/10.1002/mgg3.1866
Verkko-osoite: https://onlinelibrary.wiley.com/doi/10.1002/mgg3.1866
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/175034215
Background: The genetic architecture of hearing impairment in Finland is largely unknown. Here, we investigated two Finnish families with autosomal recessive nonsyndromic symmetrical moderate-to-severe hearing impairment.
Methods: Exome and custom capture next-generation sequencing were used to detect the underlying cause of hearing impairment.
Results: In both Finnish families, we identified a homozygous pathogenic splice site variant c.637+1G>T in CAPB2 that is known to cause autosomal recessive nonsyndromic hearing impairment. Four CABP2 variants have been reported to underlie autosomal recessive nonsyndromic hearing impairment in eight families from Iran, Turkey, Pakistan, Italy, and Denmark. Of these variants, the pathogenic splice site variant c.637+1G>T is the most prevalent. The c.637+1G>T variant is enriched in the Finnish population, which has undergone multiple bottlenecks that can lead to the higher frequency of certain variants including those involved in disease.
Conclusion: We report two Finnish families with hearing impairment due to the CABP2 splice site variant c.637+1G>T.
Ladattava julkaisu This is an electronic reprint of the original article. |  |
