Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families

P. Gasparini, Xavier P. Estivill, V. Volpini, A. Totaro, S. Castellvi-Bel, N. Govea, M. Mila, M. Della Monica, V. Ventruto, M. De Benedetto, P. Stanziale, L. Zelante, E. S. Mansfield, Lodewijk Sandkuijl, S. Surrey, P. Fortina

Research output: Contribution to journalArticle

106 Citations (Scopus)

Abstract

Recent studies show a susceptibility locus (DFNB1) responsible for non-syndromic neurosensory autosomal-recessive deafness (NSRD) mapping to the pericentromeric region of chromosome 13q. In order to better understand the frequency with which DFNB1 is the gene for deafness in our patient population and the role of DFNB1 in Caucasians, we performed a genetic linkage study with four microsatellite markers linked to DFNB1 in a total of 48 independent Mediterranean families, of which 30 and 18 were of Italian and Spanish descent, respectively. A maximum two-point lod score of 7.28 was found with marker D13S115 at a recombination frequency of Θ 0.1. Significant lod scores were also obtained for D13S143, D13S292 and D13S175. Genetic heterogeneity was confirmed using the HOMOG program which indicated absence of linkage to DFNB1 in approximately 21% of the sample. This study clearly demonstrates that DFNB1 plays an important role in 79% of Mediterranean families with NSRD. Furthermore, results from multipoint analysis predict that the DFNB1 gene maps between markers D13S175 and D13S115 which are separated by approximately 14.2 cM.

Original languageEnglish
Pages (from-to)83-88
Number of pages6
JournalEuropean Journal of Human Genetics
Volume5
Issue number2
Publication statusPublished - Mar 1997
Externally publishedYes

Fingerprint

Lod Score
Genetic Linkage
Genetic Heterogeneity
Deafness
Microsatellite Repeats
Genetic Recombination
Genes
Chromosomes
Population
Autosomal Recessive Deafness

Keywords

  • Dinucleotide repeat polymorphism
  • Hearing loss
  • Linkage analysis
  • Non-syndromic neurosensory autosomal-recessive deafness

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Gasparini, P., Estivill, X. P., Volpini, V., Totaro, A., Castellvi-Bel, S., Govea, N., ... Fortina, P. (1997). Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families. European Journal of Human Genetics, 5(2), 83-88.

Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families. / Gasparini, P.; Estivill, Xavier P.; Volpini, V.; Totaro, A.; Castellvi-Bel, S.; Govea, N.; Mila, M.; Della Monica, M.; Ventruto, V.; De Benedetto, M.; Stanziale, P.; Zelante, L.; Mansfield, E. S.; Sandkuijl, Lodewijk; Surrey, S.; Fortina, P.

In: European Journal of Human Genetics, Vol. 5, No. 2, 03.1997, p. 83-88.

Research output: Contribution to journalArticle

Gasparini, P, Estivill, XP, Volpini, V, Totaro, A, Castellvi-Bel, S, Govea, N, Mila, M, Della Monica, M, Ventruto, V, De Benedetto, M, Stanziale, P, Zelante, L, Mansfield, ES, Sandkuijl, L, Surrey, S & Fortina, P 1997, 'Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families', European Journal of Human Genetics, vol. 5, no. 2, pp. 83-88.
Gasparini, P. ; Estivill, Xavier P. ; Volpini, V. ; Totaro, A. ; Castellvi-Bel, S. ; Govea, N. ; Mila, M. ; Della Monica, M. ; Ventruto, V. ; De Benedetto, M. ; Stanziale, P. ; Zelante, L. ; Mansfield, E. S. ; Sandkuijl, Lodewijk ; Surrey, S. ; Fortina, P. / Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families. In: European Journal of Human Genetics. 1997 ; Vol. 5, No. 2. pp. 83-88.
@article{8ba9e45af97e4a5aa7d40fa916333343,
title = "Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families",
abstract = "Recent studies show a susceptibility locus (DFNB1) responsible for non-syndromic neurosensory autosomal-recessive deafness (NSRD) mapping to the pericentromeric region of chromosome 13q. In order to better understand the frequency with which DFNB1 is the gene for deafness in our patient population and the role of DFNB1 in Caucasians, we performed a genetic linkage study with four microsatellite markers linked to DFNB1 in a total of 48 independent Mediterranean families, of which 30 and 18 were of Italian and Spanish descent, respectively. A maximum two-point lod score of 7.28 was found with marker D13S115 at a recombination frequency of Θ 0.1. Significant lod scores were also obtained for D13S143, D13S292 and D13S175. Genetic heterogeneity was confirmed using the HOMOG program which indicated absence of linkage to DFNB1 in approximately 21{\%} of the sample. This study clearly demonstrates that DFNB1 plays an important role in 79{\%} of Mediterranean families with NSRD. Furthermore, results from multipoint analysis predict that the DFNB1 gene maps between markers D13S175 and D13S115 which are separated by approximately 14.2 cM.",
keywords = "Dinucleotide repeat polymorphism, Hearing loss, Linkage analysis, Non-syndromic neurosensory autosomal-recessive deafness",
author = "P. Gasparini and Estivill, {Xavier P.} and V. Volpini and A. Totaro and S. Castellvi-Bel and N. Govea and M. Mila and {Della Monica}, M. and V. Ventruto and {De Benedetto}, M. and P. Stanziale and L. Zelante and Mansfield, {E. S.} and Lodewijk Sandkuijl and S. Surrey and P. Fortina",
year = "1997",
month = "3",
language = "English",
volume = "5",
pages = "83--88",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
number = "2",

}

TY - JOUR

T1 - Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families

AU - Gasparini, P.

AU - Estivill, Xavier P.

AU - Volpini, V.

AU - Totaro, A.

AU - Castellvi-Bel, S.

AU - Govea, N.

AU - Mila, M.

AU - Della Monica, M.

AU - Ventruto, V.

AU - De Benedetto, M.

AU - Stanziale, P.

AU - Zelante, L.

AU - Mansfield, E. S.

AU - Sandkuijl, Lodewijk

AU - Surrey, S.

AU - Fortina, P.

PY - 1997/3

Y1 - 1997/3

N2 - Recent studies show a susceptibility locus (DFNB1) responsible for non-syndromic neurosensory autosomal-recessive deafness (NSRD) mapping to the pericentromeric region of chromosome 13q. In order to better understand the frequency with which DFNB1 is the gene for deafness in our patient population and the role of DFNB1 in Caucasians, we performed a genetic linkage study with four microsatellite markers linked to DFNB1 in a total of 48 independent Mediterranean families, of which 30 and 18 were of Italian and Spanish descent, respectively. A maximum two-point lod score of 7.28 was found with marker D13S115 at a recombination frequency of Θ 0.1. Significant lod scores were also obtained for D13S143, D13S292 and D13S175. Genetic heterogeneity was confirmed using the HOMOG program which indicated absence of linkage to DFNB1 in approximately 21% of the sample. This study clearly demonstrates that DFNB1 plays an important role in 79% of Mediterranean families with NSRD. Furthermore, results from multipoint analysis predict that the DFNB1 gene maps between markers D13S175 and D13S115 which are separated by approximately 14.2 cM.

AB - Recent studies show a susceptibility locus (DFNB1) responsible for non-syndromic neurosensory autosomal-recessive deafness (NSRD) mapping to the pericentromeric region of chromosome 13q. In order to better understand the frequency with which DFNB1 is the gene for deafness in our patient population and the role of DFNB1 in Caucasians, we performed a genetic linkage study with four microsatellite markers linked to DFNB1 in a total of 48 independent Mediterranean families, of which 30 and 18 were of Italian and Spanish descent, respectively. A maximum two-point lod score of 7.28 was found with marker D13S115 at a recombination frequency of Θ 0.1. Significant lod scores were also obtained for D13S143, D13S292 and D13S175. Genetic heterogeneity was confirmed using the HOMOG program which indicated absence of linkage to DFNB1 in approximately 21% of the sample. This study clearly demonstrates that DFNB1 plays an important role in 79% of Mediterranean families with NSRD. Furthermore, results from multipoint analysis predict that the DFNB1 gene maps between markers D13S175 and D13S115 which are separated by approximately 14.2 cM.

KW - Dinucleotide repeat polymorphism

KW - Hearing loss

KW - Linkage analysis

KW - Non-syndromic neurosensory autosomal-recessive deafness

UR - http://www.scopus.com/inward/record.url?scp=12644276408&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=12644276408&partnerID=8YFLogxK

M3 - Article

VL - 5

SP - 83

EP - 88

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 2

ER -