Literature DB >> 23856930

Phacomatosis pigmentokeratotica is a "pseudodidymosis".

Rudolf Happle1.   

Abstract

In phacomatosis pigmentokeratotica, papular nevus spilus coexists with nevus sebaceus. The disorder was thought to be a didymosis with early postzygotic recombination. In this issue, however, Groesser and co-workers provide a new concept. Both nevi originate from a single heterozygous HRAS mutation in a pluripotent progenitor cell. This new understanding has implications for other proposed examples of didymosis in humans.

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Year:  2013        PMID: 23856930     DOI: 10.1038/jid.2013.74

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  5 in total

1.  Photoletter to the editor: A neurocutaneous rarity: phacomatosis pigmentokeratotica.

Authors:  Thiago Cardoso Vale; David Márcio Barbosa Santos; Ricardo Oliveira Maciel; Francisco Cardoso; Rudolf Happle
Journal:  J Dermatol Case Rep       Date:  2014-06-30

2.  Epidermal, sebaceous, and melanocytic nevoid proliferations are spectrums of mosaic RASopathies.

Authors:  Su Luo; Hensin Tsao
Journal:  J Invest Dermatol       Date:  2014-10       Impact factor: 8.551

3.  Vascular malformation and common keratinocytic nevus of the soft type: phacomatosis pigmentovascularis revisited.

Authors:  André Laureano; Rodrigo Carvalho; Cristina Amaro; Isabel Freitas; Jorge Cardoso
Journal:  Case Rep Dermatol Med       Date:  2014-11-23

4.  Phacomatosis pigmentokeratotica or the Schimmelpenning-Feuerstein-Mims syndrome?

Authors:  Boris N Gamayunov; Nikolay G Korotkiy; Elena E Baranova
Journal:  Clin Case Rep       Date:  2016-05-04

5.  An Early Description of a "Human Mosaic" Involving the Skin: A Story from 1945.

Authors:  Rudolf Happle
Journal:  Acta Derm Venereol       Date:  2020-03-25       Impact factor: 3.875

  5 in total

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