Poikiloderma a varied presentation - Huriez syndrome

Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.

Detalles Bibliográficos
Autores principales: Kharge, Priyadarshini, Fernendes, Carol, Jairath, Vijayeeta, Mohan, Madan, Chandra, Suresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314883/
https://www.ncbi.nlm.nih.gov/pubmed/25657913
http://dx.doi.org/10.4103/2229-5178.148929
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author Kharge, Priyadarshini
Fernendes, Carol
Jairath, Vijayeeta
Mohan, Madan
Chandra, Suresh
author_facet Kharge, Priyadarshini
Fernendes, Carol
Jairath, Vijayeeta
Mohan, Madan
Chandra, Suresh
author_sort Kharge, Priyadarshini
collection PubMed
description Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.
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spelling pubmed-43148832015-02-05 Poikiloderma a varied presentation - Huriez syndrome Kharge, Priyadarshini Fernendes, Carol Jairath, Vijayeeta Mohan, Madan Chandra, Suresh Indian Dermatol Online J Case Report Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4314883/ /pubmed/25657913 http://dx.doi.org/10.4103/2229-5178.148929 Text en Copyright: © Indian Dermatology Online Journal 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kharge, Priyadarshini
Fernendes, Carol
Jairath, Vijayeeta
Mohan, Madan
Chandra, Suresh
Poikiloderma a varied presentation - Huriez syndrome
title Poikiloderma a varied presentation - Huriez syndrome
title_full Poikiloderma a varied presentation - Huriez syndrome
title_fullStr Poikiloderma a varied presentation - Huriez syndrome
title_full_unstemmed Poikiloderma a varied presentation - Huriez syndrome
title_short Poikiloderma a varied presentation - Huriez syndrome
title_sort poikiloderma a varied presentation - huriez syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314883/
https://www.ncbi.nlm.nih.gov/pubmed/25657913
http://dx.doi.org/10.4103/2229-5178.148929
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