Literature DB >> 8571965

Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.

J E Reynolds1, M L Marazita, J M Meyer, C A Stevens, L J Eaves, K S Arnos, L M Ploughman, C MacLean, W E Nance, S R Diehl.   

Abstract

We used segregation analysis to investigate the genetic basis of variation in dystopia canthorum, one of the key diagnostic features of Waardenburg syndrome type 1 (WS1). We sought to determine whether the W-index, a quantitative measure of this craniofacial feature, is influenced primarily either by allelic variation in the PAX3 disease gene or other major loci, by polygenic background effects, or by all of these potential sources of genetic variation. We studied both WS1-affected individuals and their WS1-unaffected relatives. After adjustment of the W-index for WS1 disease status, segregation analyses by the regression approach indicated major-locus control of this variation, although residual parent-offspring and sib-sib correlations are consistent with additional (possibly polygenic) effects. Separate analyses of WS1-affected and WS1-unaffected individuals suggest that epistatic interactions between disease alleles at the PAX3 WS1 locus and a second major locus influence variation in dystopia canthorum. Our approach should be applicable for assessing the genetic architecture of variation associated with other genetic diseases.

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Year:  1996        PMID: 8571965      PMCID: PMC1914540     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  13 in total

1.  A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Authors:  P J WAARDENBURG
Journal:  Am J Hum Genet       Date:  1951-09       Impact factor: 11.025

2.  Equivalence of the mixed and regressive models for genetic analysis. I. Continuous traits.

Authors:  F M Demenais; G E Bonney
Journal:  Genet Epidemiol       Date:  1989       Impact factor: 2.135

3.  Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3.

Authors:  D J Epstein; M Vekemans; P Gros
Journal:  Cell       Date:  1991-11-15       Impact factor: 41.582

4.  Analysis of locus heterogeneity in Waardenburg syndrome types 1 and 2 using highly informative microsatellite markers.

Authors:  J E Reynolds; K S Arnos; B Landa; C A Stevens; B A Salbert; L Wright; B Duke; W Hunt; M L Marazita; L Ploughman
Journal:  Hum Hered       Date:  1995 Sep-Oct       Impact factor: 0.444

5.  An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes.

Authors:  D F Easton; M A Ponder; S M Huson; B A Ponder
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

6.  Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors:  C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

7.  Apparent non-penetrance for dystopia in Waardenburg syndrome type I, with some hints on the diagnosis of dystopia canthorum.

Authors:  S Arias; M Mota
Journal:  J Genet Hum       Date:  1978-06

Review 8.  Heterogeneity in Waardenburg syndrome.

Authors:  M J Hageman; J W Delleman
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

9.  Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Authors:  L A Farrer; K S Arnos; J H Asher; C T Baldwin; S R Diehl; T B Friedman; J Greenberg; K M Grundfast; C Hoth; A K Lalwani
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

10.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

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  2 in total

1.  [Screening for ocular involvement in deaf children].

Authors:  Belghmaidi Sarah; Belhoucha Btissam; Hajji Ibtissam; Rochdi Youssef; Albab Nabil; Nouri Hassan; Aderdour Lahcen; Raji Abdelaziz; Moutaouakil Abdeljalil
Journal:  Pan Afr Med J       Date:  2019-07-05

2.  A Novel Spontaneous Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type II.

Authors:  Sen Chen; Yuan Jin; Le Xie; Wen Xie; Kai Xu; Yue Qiu; Xue Bai; Hui-Min Zhang; Xiao-Zhou Liu; Xiao-Hui Wang; Wei-Jia Kong; Yu Sun
Journal:  Neural Plast       Date:  2020-08-28       Impact factor: 3.599

  2 in total

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