PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease

Hidradenitis suppurativa is a chronic relapsing disease with multiple abscesses, nodules, and scars in the apocrine bearing areas. Dowling-Degos is a rare autosomal dominant genodermatosis characterized by multiple hyperpigmented macules or papules in reticulate pattern, affecting mainly the flexure...

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Autores principales: Peter, Dincy C. V., Smith, Frances J. D., Wilson, Neil J., Danda, Sumita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982026/
https://www.ncbi.nlm.nih.gov/pubmed/33768038
http://dx.doi.org/10.4103/idoj.IDOJ_218_20
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author Peter, Dincy C. V.
Smith, Frances J. D.
Wilson, Neil J.
Danda, Sumita
author_facet Peter, Dincy C. V.
Smith, Frances J. D.
Wilson, Neil J.
Danda, Sumita
author_sort Peter, Dincy C. V.
collection PubMed
description Hidradenitis suppurativa is a chronic relapsing disease with multiple abscesses, nodules, and scars in the apocrine bearing areas. Dowling-Degos is a rare autosomal dominant genodermatosis characterized by multiple hyperpigmented macules or papules in reticulate pattern, affecting mainly the flexures. We report a case of coexisting hidradenitis suppurativa and Dowling-Degos disease in a 31-year-old male in whom PSENEN mutation analysis revealed a splice site mutation c.62-1G>T.
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spelling pubmed-79820262021-03-24 PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease Peter, Dincy C. V. Smith, Frances J. D. Wilson, Neil J. Danda, Sumita Indian Dermatol Online J Case Report Hidradenitis suppurativa is a chronic relapsing disease with multiple abscesses, nodules, and scars in the apocrine bearing areas. Dowling-Degos is a rare autosomal dominant genodermatosis characterized by multiple hyperpigmented macules or papules in reticulate pattern, affecting mainly the flexures. We report a case of coexisting hidradenitis suppurativa and Dowling-Degos disease in a 31-year-old male in whom PSENEN mutation analysis revealed a splice site mutation c.62-1G>T. Wolters Kluwer - Medknow 2020-09-28 /pmc/articles/PMC7982026/ /pubmed/33768038 http://dx.doi.org/10.4103/idoj.IDOJ_218_20 Text en Copyright: © 2021 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Peter, Dincy C. V.
Smith, Frances J. D.
Wilson, Neil J.
Danda, Sumita
PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease
title PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease
title_full PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease
title_fullStr PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease
title_full_unstemmed PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease
title_short PSENEN Mutation in Coexistent Hidradenitis Suppurativa and Dowling-Degos Disease
title_sort psenen mutation in coexistent hidradenitis suppurativa and dowling-degos disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982026/
https://www.ncbi.nlm.nih.gov/pubmed/33768038
http://dx.doi.org/10.4103/idoj.IDOJ_218_20
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