Lipoid proteinosis: A review with two case reports

Vishal Kabre; Smitha Rani; Keerthilatha M. Pai; Sakshi Kamra

doi:10.4103/0976-237X.156053

Lipoid proteinosis: A review with two case reports

Vishal Kabre
, Smitha Rani
, Keerthilatha M. Pai
, Sakshi Kamra^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

19 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	233-236
Number of pages	4
Journal	Contemporary Clinical Dentistry
Volume	6
Issue number	2
DOIs	https://doi.org/10.4103/0976-237X.156053
Publication status	Published - 01-01-2015

All Science Journal Classification (ASJC) codes

Orthodontics
Oral Surgery
Periodontics

Access to Document

10.4103/0976-237X.156053

Cite this

@article{e8d6ea74c34f45f28a753128a4a7c210,

title = "Lipoid proteinosis: A review with two case reports",

abstract = "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.",

author = "Vishal Kabre and Smitha Rani and Pai, \{Keerthilatha M.\} and Sakshi Kamra",

year = "2015",

month = jan,

day = "1",

doi = "10.4103/0976-237X.156053",

language = "English",

volume = "6",

pages = "233--236",

journal = "Contemporary Clinical Dentistry",

issn = "0976-237X",

publisher = "Wolters Kluwer Medknow Publications",

number = "2",

}

TY - JOUR

T1 - Lipoid proteinosis

T2 - A review with two case reports

AU - Kabre, Vishal

AU - Rani, Smitha

AU - Pai, Keerthilatha M.

AU - Kamra, Sakshi

PY - 2015/1/1

Y1 - 2015/1/1

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/84928991748

UR - https://www.scopus.com/pages/publications/84928991748#tab=citedBy

U2 - 10.4103/0976-237X.156053

DO - 10.4103/0976-237X.156053

M3 - Article

AN - SCOPUS:84928991748

SN - 0976-237X

VL - 6

SP - 233

EP - 236

JO - Contemporary Clinical Dentistry

JF - Contemporary Clinical Dentistry

IS - 2

ER -

Lipoid proteinosis: A review with two case reports

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this