Results 11 to 20 of about 1,553 (193)
Oral manifestations of lipoid proteinosis: A case report and literature review
Saudi Dental Journal, 2013 Lipoid proteinosis is an uncommon autosomal recessive metabolic disorder that presents in early life with hoarseness and pox-like acneiform scars involving the skin and mucous membranes.
S.M. Ravi Prakash +3 more
doaj +3 more sources
Lipoid proteinosis: A rare entity.
Indian J Ophthalmol, 2015 Urbach–Wiethe syndrome or lipoid proteinosis is a rare autosomal recessive disorder characterized histologically by infiltration of Periodic acid Schiff-positive hyaline material in the skin, upper aerodigestive tract, eyelids, and internal organs ...
Mukherjee B, Devi PN.
europepmc +2 more sources
Lipoid proteinosis: Unfamiliar skin findings delay diagnosis. [PDF]
JAAD Case Rep, 2018 Lipoid proteinosis (LP) is a rare, inherited condition that progresses gradually with multisystemic manifestations. Histopathologic characteristics can be understated, delaying the diagnosis if a high degree of suspicion is not ...
Larkin S +5 more
europepmc +3 more sources
Lipoid proteinosis: a rare encounter in dental office. [PDF]
Case Rep Dent, 2015 Lipoid proteinosis is a sporadic congenital metabolic disorder which is characterized by deposition of hyaline material in dermis, submucosal connective tissue, and various internal organs. It has an extremely low prevalence rate with less than 300 cases
Deshpande P +5 more
europepmc +2 more sources
Lipoid Proteinosis; A Case Report with Difficult Intubation [PDF]
JLUMHS, 2018 Lipoid proteinosis is an autosomal recessive disorder and caused by the mutations of ECM1 (extracellular matrix protein 1) gene on chromosome 1q21.
Syed Aftab Haider +4 more
doaj +3 more sources
Acitretin treatment for lipoid proteinosis. [PDF]
Case Rep Dermatol Med, 2012 Lipoid proteinosis (LP) is a rare, autosomal-recessive disease characterized by the hoarseness and widespread cutaneous scarring, more prominent on sun-exposed areas.
Gündüz O +3 more
europepmc +2 more sources
Association Between Lipoid Proteinosis and Coeliac Disease. [PDF]
Dermatol Pract Concept, 2023 Bendaoud L, Bigjoine I, Hocar O, Amal S.
europepmc +2 more sources
Lipoid proteinosis: A review with two case reports.
Contemp Clin Dent, 2015 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 ...
Kabre V, Rani S, Pai KM, Kamra S.
europepmc +2 more sources
Lipoid proteinosis (Urbach-Wiethe disease) in two siblings.
Indian Dermatol Online J, 2014 Lipoid proteinosis is a very rare autosomal recessive disorder characterized by deposition of hyaline material in the skin and the upper aerodigestive tract. Hoarseness of voice occurs very early in life and airway obstruction may occur.
Thaddanee R +3 more
europepmc +2 more sources