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.
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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 -