Literature DB >> 162071

[Scleroatrophying and degenerative keratodermic genodermatosis of the extremities].

M Shaw, E Formentini, A R de Kaminsky, C A Kaminsky, J Abulafia.   

Abstract

A case of a picture described by Huriez et al. under the title of scleatrophying and keratodermic genodermatosis of the limbs usually degenerative is presented. In the genealogic study it was observed that seven out of the sixteen members that belonged to this primary family group were affected or probably affected and it is stressed that one of them died from metastasis of spinocellular epithelioma.

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Year:  1978        PMID: 162071

Source DB:  PubMed          Journal:  Med Cutan Ibero Lat Am        ISSN: 0210-5187


  1 in total

1.  A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23.

Authors:  Y A Lee; H P Stevens; E Delaporte; U Wahn; A Reis
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

  1 in total

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