Cargando…

Pachyonychia Congenita Type 1: Case Report and Review of the Literature

The case of an 8-year-old boy is hereby reported, who presented with nail dystrophy, subungual hyperkeratosis, oral leukokeratosis, and numerous follicular papules all over the body. The features were consistent with a diagnosis of pachyonychia congenita type 1. The case is being reported for its ra...

Descripción completa

Detalles Bibliográficos
Autores principales: Rathore, Praveen Kumar, Khullar, Varun, Das, Anupam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817447/
https://www.ncbi.nlm.nih.gov/pubmed/27057022
http://dx.doi.org/10.4103/0019-5154.177761
_version_ 1782424888454152192
author Rathore, Praveen Kumar
Khullar, Varun
Das, Anupam
author_facet Rathore, Praveen Kumar
Khullar, Varun
Das, Anupam
author_sort Rathore, Praveen Kumar
collection PubMed
description The case of an 8-year-old boy is hereby reported, who presented with nail dystrophy, subungual hyperkeratosis, oral leukokeratosis, and numerous follicular papules all over the body. The features were consistent with a diagnosis of pachyonychia congenita type 1. The case is being reported for its rarity. We also discuss in a nutshell, the literature till date.
format Online
Article
Text
id pubmed-4817447
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-48174472016-04-07 Pachyonychia Congenita Type 1: Case Report and Review of the Literature Rathore, Praveen Kumar Khullar, Varun Das, Anupam Indian J Dermatol Case Report The case of an 8-year-old boy is hereby reported, who presented with nail dystrophy, subungual hyperkeratosis, oral leukokeratosis, and numerous follicular papules all over the body. The features were consistent with a diagnosis of pachyonychia congenita type 1. The case is being reported for its rarity. We also discuss in a nutshell, the literature till date. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4817447/ /pubmed/27057022 http://dx.doi.org/10.4103/0019-5154.177761 Text en Copyright: © 2016 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Rathore, Praveen Kumar
Khullar, Varun
Das, Anupam
Pachyonychia Congenita Type 1: Case Report and Review of the Literature
title Pachyonychia Congenita Type 1: Case Report and Review of the Literature
title_full Pachyonychia Congenita Type 1: Case Report and Review of the Literature
title_fullStr Pachyonychia Congenita Type 1: Case Report and Review of the Literature
title_full_unstemmed Pachyonychia Congenita Type 1: Case Report and Review of the Literature
title_short Pachyonychia Congenita Type 1: Case Report and Review of the Literature
title_sort pachyonychia congenita type 1: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817447/
https://www.ncbi.nlm.nih.gov/pubmed/27057022
http://dx.doi.org/10.4103/0019-5154.177761
work_keys_str_mv AT rathorepraveenkumar pachyonychiacongenitatype1casereportandreviewoftheliterature
AT khullarvarun pachyonychiacongenitatype1casereportandreviewoftheliterature
AT dasanupam pachyonychiacongenitatype1casereportandreviewoftheliterature