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...
Main Authors: | Vishal Kabre, Smitha Rani, Keerthilatha M Pai, Sakshi Kamra |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2015-01-01
|
Series: | Contemporary Clinical Dentistry |
Subjects: | |
Online Access: | http://www.contempclindent.org/article.asp?issn=0976-237X;year=2015;volume=6;issue=2;spage=233;epage=236;aulast=Kabre |
Similar Items
-
Novel compound heterozygous mutations of ECM1 in a Chinese family with lipoid proteinosis
by: Wei Wu, et al.
Published: (2019-01-01) -
Novel Mutations in Extracellular Matrix Protein 1 Gene in a Chinese Patient with Lipoid Proteinosis
by: Xiao Bai, et al.
Published: (2016-01-01) -
Extracellular matrix protein 1 gene mutation in turkish patients with lipoid proteinosis
by: Selma Bakar Dertlioğlu, et al.
Published: (2019-01-01) -
Lipoid proteinosis in two siblings
by: Behera Samira Kumar, et al.
Published: (2006-01-01) -
Lipoid proteinosis
by: Mukhija Pooja, et al.
Published: (2006-01-01)