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Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.

Authors
 Mee Hyun Song  ;  Joong-Wook Shin  ;  Hong-Joon Park  ;  Kyung-A Lee  ;  Yoonjung Kim  ;  Un-Kyung Kim  ;  Ju Hyun Jeon  ;  Jae Young Choi 
Citation
 Laryngoscope, Vol.124(5) : 194-202, 2014 
Journal Title
 Laryngoscope 
ISSN
 0023-852X 
Issue Date
2014
MeSH
Adolescent ; Adult ; Alleles ; Asian Continental Ancestry Group/genetics ; Audiometry, Pure-Tone ; Child ; Child, Preschool ; Female ; Genotype ; Hearing Loss/genetics* ; Hearing Loss, Sensorineural/genetics* ; Humans ; Infant ; Male ; Membrane Transport Proteins/genetics* ; Mutation ; Phenotype ; Polymerase Chain Reaction ; Republic of Korea ; Retrospective Studies ; Vestibular Aqueduct/abnormalities*
Keywords
SLC26A4 ; enlarged vestibular aqueduct ; hearing loss ; mutation ; variability
Abstract
OBJECTIVES/HYPOTHESIS: Enlarged vestibular aqueduct (EVA) and hearing loss are known to be caused by SLC26A4 mutations, but large phenotypic variability exists among patients with biallelic SLC26A4 mutations. Intrafamilial phenotypic variability was analyzed in multiplex EVA families carrying biallelic SLC26A4 mutations to identify the contribution of SLC26A4 mutations and other genetic or environmental factors influencing the clinical manifestations. STUDY DESIGN: Retrospective case series. METHODS: Eleven multiplex Korean families with EVA and hearing loss that carry biallelic mutations of the SLC26A4 gene were included. Genetic analysis for SLC26A4 and other genes including FOXI1, FOXI1-DBD, and KCNJ10 was performed. The auditory and other phenotypes were compared among siblings with the same SLC26A4 mutations. RESULTS: The difference in the auditory phenotypes was identified between siblings in approximately half of the EVA families. Families with SLC26A4 mutations other than H723R homozygous mutations demonstrated more phenotypic variability, especially in those carrying IVS7-2A>G splice site mutation. Cochlear malformation was a consistent finding among siblings with the same SLC26A4 mutations. No mutation was identified in the FOXI1, FOXI1-DBD, and KCNJ10 genes in the tested families. CONCLUSIONS: The possibility of variability concerning auditory phenotype should be considered even within family members carrying the same SLC26A4 mutations when providing genetic counseling to multiplex EVA families. Mutations in the currently known genes associated with EVA other than SLC26A4 were not found to be responsible for the intrafamilial phenotypic variability. Modifier genes or environmental factors other than the currently known genes seem to play a role in the phenotypic expressions of EVA patients.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/lary.24504/abstract
DOI
10.1002/lary.24504
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
Yonsei Authors
Lee, Kyung A(이경아) ORCID logo https://orcid.org/0000-0001-5320-6705
Choi, Jae Young(최재영) ORCID logo https://orcid.org/0000-0001-9493-3458
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/98651
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