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Lipoid proteinosis: A review with two case reports
Lipoid proteinosis (LP) is a rare autosomal recessive genodermatoses characterized by deposition of amorphous hyaline material in different parts of the body, especially the skin, mucous membranes of the upper aerodigestive tract, and internal organs. Oral cavity is most extensively affected area by...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456748/ https://www.ncbi.nlm.nih.gov/pubmed/26097361 http://dx.doi.org/10.4103/0976-237X.156053 |
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author | Kabre, Vishal Rani, Smitha Pai, Keerthilatha M. Kamra, Sakshi |
author_facet | Kabre, Vishal Rani, Smitha Pai, Keerthilatha M. Kamra, Sakshi |
author_sort | Kabre, Vishal |
collection | PubMed |
description | Lipoid proteinosis (LP) is a rare autosomal recessive genodermatoses characterized by deposition of amorphous hyaline material in different parts of the body, especially the skin, mucous membranes of the upper aerodigestive tract, and internal organs. Oral cavity is most extensively affected area by the disease. This paper reports two classic cases of LP with oral manifestations but without a history of consanguinity along with a concise review of the literature on the disease. |
format | Online Article Text |
id | pubmed-4456748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44567482015-06-19 Lipoid proteinosis: A review with two case reports Kabre, Vishal Rani, Smitha Pai, Keerthilatha M. Kamra, Sakshi Contemp Clin Dent Case Report Lipoid proteinosis (LP) is a rare autosomal recessive genodermatoses characterized by deposition of amorphous hyaline material in different parts of the body, especially the skin, mucous membranes of the upper aerodigestive tract, and internal organs. Oral cavity is most extensively affected area by the disease. This paper reports two classic cases of LP with oral manifestations but without a history of consanguinity along with a concise review of the literature on the disease. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4456748/ /pubmed/26097361 http://dx.doi.org/10.4103/0976-237X.156053 Text en Copyright: © Contemporary Clinical Dentistry 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 Kabre, Vishal Rani, Smitha Pai, Keerthilatha M. Kamra, Sakshi Lipoid proteinosis: A review with two case reports |
title | Lipoid proteinosis: A review with two case reports |
title_full | Lipoid proteinosis: A review with two case reports |
title_fullStr | Lipoid proteinosis: A review with two case reports |
title_full_unstemmed | Lipoid proteinosis: A review with two case reports |
title_short | Lipoid proteinosis: A review with two case reports |
title_sort | lipoid proteinosis: a review with two case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456748/ https://www.ncbi.nlm.nih.gov/pubmed/26097361 http://dx.doi.org/10.4103/0976-237X.156053 |
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