Literature DB >> 20096200

Superimposed segmental manifestation of both rare and common cutaneous disorders: a new paradigm.

R Happle1.   

Abstract

In autosomal dominant skin disorders, a superimposed mosaic involvement arranged in a linear or otherwise segmental pattern is sometimes noted. Molecular proof of such type 2 segmental manifestation has so far been provided in Hailey-Hailey disease and Cowden syndrome. A similar superimposed segmental involvement can be found in numerous common disorders with a polygenic background, such a psoriasis, lichen planus, or vitiligo. In polygenic diseases, however, we can never recognize with certainty a type 1 segmental manifestation, which is why we should use more neutral terms in the form of isolated versus superimposed segmental involvement. In the near future, the new paradigm of superimposed segmental manifestation may hopefully help elucidate the molecular basis of both monogenic and polygenic skin disorders.

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Year:  2009        PMID: 20096200     DOI: 10.1016/s0001-7310(09)73171-0

Source DB:  PubMed          Journal:  Actas Dermosifiliogr        ISSN: 0001-7310


  5 in total

Review 1.  Neurocutaneous Manifestations of Genetic Mosaicism.

Authors:  Maurice A M van Steensel
Journal:  J Pediatr Genet       Date:  2015-11-30

Review 2.  The role of the ATP2C1 gene in Hailey-Hailey disease.

Authors:  Hao Deng; Heng Xiao
Journal:  Cell Mol Life Sci       Date:  2017-05-27       Impact factor: 9.261

3.  A case of linear porokeratosis superimposed on disseminated superficial actinic porokeratosis.

Authors:  Rebecca Löhrer; Aysegül Neumann-Acikel; Rüdiger Eming; Karin Hartmann; Heinrich Rasokat; Thomas Krieg; Rudolf Happle; Sabine Eming
Journal:  Case Rep Dermatol       Date:  2010-08-06

Review 4.  Cutaneous mosaicisms: concepts, patterns and classifications.

Authors:  Samara Silva Kouzak; Marcela Sena Teixeira Mendes; Izelda Maria Carvalho Costa
Journal:  An Bras Dermatol       Date:  2013 Jul-Aug       Impact factor: 1.896

5.  Superimposed Segmental Manifestation of Juvenile Amyopathic Dermatomyositis in a 9-year-old Boy.

Authors:  Isil Bulur; Hilal Kaya Erdogan; Zeynep Nurhan Saracoglu; Rudolf Happle; Funda Canaz
Journal:  Indian J Dermatol       Date:  2017 Jul-Aug       Impact factor: 1.494

  5 in total

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