Literature DB >> 1248830

[Dermatoglyphics of homo- and heterozygotes for Wilson's disease (hepatolenticular degeneration) (author's transl)].

W Vormittag, M Weninger, R Willvonseder, F Wewalka.   

Abstract

Dermatoglyphics of 11 patients with Wilson's disease and 16 of their clinically asymptomatic relatives of first degree were investigated; 11 of the latter ones were heterozygous in agreement with the turn over rates of Cu-67, 12 under the assumption of autosomal recessive inheritance. On the finger tips the Mb. Wilson patients showed 52.7% whorls, their heterozygous relatives about 40%; compared with our controls (males 33.16%, females 28.82%, Aue-Hauser, 1970) that means a strong increase of this pattern type. On the palm the high frequency of hypothenar patterns in homo- and heterozygotes for Wilson's disease and of loops with accessory triradius in the 4th interdigitum of the patients with Wilson's disease was striking.

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Year:  1976        PMID: 1248830     DOI: 10.1007/bf00296148

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  6 in total

1.  Relationship between fingerprint patterns and Wilson's disease.

Authors:  R E HODGES; J R SIMON
Journal:  J Lab Clin Med       Date:  1962-10

2.  Long-term body retention of radiocopper (67Cu) and the diagnosis of Wilson's disease.

Authors:  R Willvonseder; N P Goldstein; W N Tauxe
Journal:  Mayo Clin Proc       Date:  1974-06       Impact factor: 7.616

3.  [Relationship between dermatoglyphics and Wilson's disease].

Authors:  W Vormittag; M Weninger; H Hayek
Journal:  Humangenetik       Date:  1973

4.  A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism.

Authors:  R Willvonseder; N P Goldstein; J T McCall; R E Yoss; W N Tauxe
Journal:  Neurology       Date:  1973-10       Impact factor: 9.910

5.  A genetic study of Wilson's disease: evidence for heterogeneity.

Authors:  D W Cox; F C Fraser; A Sass-Kortsak
Journal:  Am J Hum Genet       Date:  1972-11       Impact factor: 11.025

6.  A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration).

Authors:  A G BEARN
Journal:  Ann Hum Genet       Date:  1960-04       Impact factor: 1.670

  6 in total

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