Results 71 to 80 of about 836 (156)
Lipoid Proteinosis of the Pharynx and Larynx: A Case Report
Ear, Nose & Throat JournalLipoid proteinosis (LP) is a rare inherited multisystem disease. Classical clinical features include beaded eyelid papules, laryngeal infiltration, and neurological symptoms.
Zhuojun Li BS +7 more
doaj +1 more source
Lipoid proteinosis; a rare pathology, requiring multidisciplinary input. [PDF]
BMJ Case Rep, 2023 Fenech MT, Yeo D.
europepmc +1 more source
A Case with Lipoid Proteinosis Intersected with Diabetes Mellitus - Case Report
Endocrinology Research and Practice, 2009 Lipoid proteinosis (LP) is a rare disorder inherited as an autosomal recessive trait. LP is characterized by deposition of hyaline-like material in the skin, mucous membranes, and other tissues.
Deniz Gökalp +7 more
doaj +2 more sources
Dual Diagnosis of Trichohepatoenteric Syndrome and Lipoid Proteinosis in a Turkish Child. [PDF]
Mol Syndromol, 2023 Eser HC +8 more
europepmc +1 more source
Indian journal of dermatology, venereology and leprology, 2012 A 20-year old male presented with hoarseness of voice since birth, beaded papular lesions on both eyelids, multiple hypopigmented atrophic scars on trunk and extremities and yellowish infiltrated plaques on tongue, palate and buccal mucosae. Patient was diagnosed clinically as a case of lipoid proteinosis. It was confirmed by mucosal biopsy.
M K, Shah +3 more
openaire +1 more source
Late presentation of laryngeal lipoid proteinosis: a case report and review of the literature. [PDF]
J Surg Case Rep, 2022 Alrusayyis DF +4 more
europepmc +1 more source
Assessment of dynamic thiol-disulfide homeostasis in patients with lipoid proteinosis (Urbach-Wiethe syndrome). [PDF]
Rev Assoc Med Bras (1992), 2022 Taskin S +5 more
europepmc +1 more source
Ultrastructural aspects of the skin in lipoid proteinosis (Urbach-Wiethe disease). [PDF]
An Bras Dermatol, 2021 de Almeida HL +3 more
europepmc +1 more source