Literature DB >> 21128916

Dyschromatosis symmetrica hereditaria: report of a sporadic case.

Javier Consigli1, Maria S Gómez Zanni, Luciana Ragazzini, Cristian Danielo.   

Abstract

A group of pigment disorders is included under the denomination of "dyschromatosis". Dyschromatosis symmetrica hereditaria is a dominant autosomal genodermatosis mostly reported in Eastern countries. It has been rarely reported in nonoriental races and spontaneous cases are scarce. We report a spontaneous case in the West, a boy 6 years of age, with a typical presentation and who was confused initially with vitiligo.
© 2010 The International Society of Dermatology.

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Year:  2010        PMID: 21128916     DOI: 10.1111/j.1365-4632.2010.04472.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  3 in total

1.  Dyschromatosis symmetrica hereditaria of late onset?

Authors:  Caroline Balvedi Gaiewski; Sergio Zuneda Serafini; Betina Werner; Janyana M D Deonizio
Journal:  Case Rep Dermatol Med       Date:  2014-02-04

Review 2.  Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders.

Authors:  H Alshaikh; F Alsaif; S Aldukhi
Journal:  Dermatol Res Pract       Date:  2017-10-23

3.  Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China.

Authors:  Peng Wang; Shirong Yu; Jianyong Liu; Dezhi Zhang; Xiaojing Kang
Journal:  Mol Genet Genomic Med       Date:  2019-08-18       Impact factor: 2.183

  3 in total

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