Literature DB >> 670940

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

S Arias, M Mota.   

Abstract

Two large pedigrees with Waardenburg syndrome type I (W--I), i.e. with dystopia canthorum and blepharophimosis, are described to show both the variable expressivity of dystopia canthorum, which may be confused with non-penetrance of this sign, and the possibility to firmly diagnosis it with the new biometric index W, which differentiates a dystopic from a non-dystopic or a non-apparent dystopic subject, the latter within a defined biometric range. A general discussion of the relative value of blepharophimosis and dystopia canthorum as diagnostic features in W--I is presented, to conclude on the greater value of dystopia canthorum, which can be identified with confidence in more than 96% of carriers. Empirical probabilities are given for dystopia canthorum and blepharophimosis in the general populations, based on data from the world literature, useful for all ethnic groups.

Entities:  

Mesh:

Year:  1978        PMID: 670940

Source DB:  PubMed          Journal:  J Genet Hum        ISSN: 0021-7743


  14 in total

1.  Probable loose linkage between the ABO locus and Waardenburg syndrome type I.

Authors:  S Arias; M Mota; A Yánez; M Bolivar
Journal:  Humangenetik       Date:  1975

2.  Waardenburg's syndrome.

Authors:  S Arias
Journal:  J Med Genet       Date:  1980-06       Impact factor: 6.318

3.  [Visual diagnosis: Waardenburg syndrome].

Authors:  T Hager; H-S Walter; B Seitz; B Käsmann-Kellner
Journal:  Ophthalmologe       Date:  2010-07       Impact factor: 1.059

4.  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

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

Authors:  J E Reynolds; 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
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

6.  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

7.  Waardenburg's memorial lecture: Waardenburg's syndrome.

Authors:  J François
Journal:  Int Ophthalmol       Date:  1982-05       Impact factor: 2.031

8.  EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome.

Authors:  Chuan Li; Rongyu Chen; Xin Fan; Jingsi Luo; Jiale Qian; Jin Wang; Bobo Xie; Yiping Shen; Shaoke Chen
Journal:  BMC Med Genet       Date:  2015-04-11       Impact factor: 2.103

9.  A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.

Authors:  Filiz Hazan; A Taylan Ozturk; Hamit Adibelli; Nurettin Unal; Ajlan Tukun
Journal:  Mol Vis       Date:  2013-01-29       Impact factor: 2.367

10.  Waardenburg syndrome type I: Dental phenotypes and genetic analysis of an extended family.

Authors:  L Sólia-Nasser; S-N de Aquino; L-M R Paranaíba; A Gomes; P Dos-Santos-Neto; R-D Coletta; A-F Cardoso; A-C Frota; H Martelli-Júnior
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2016-05-01
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