Results 101 to 110 of about 332 (125)
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Lipoid proteinosis Urbach-Wiethe’s Disease

A 25-year-old female patient was admitted to our outpatient clinic with postpartum hoarseness. Punch biopsy specimens obtained from the larynx and sublingual region revealed multi-folded squamous epithelium with a hyperkeratosis pattern and amorphous hyaline material aggregation. This aggregation was also remarkable around the vessels.
KARAMAN, Hatice   +3 more
openaire   +1 more source

XXIX Lipoid Proteinosis (Urbach-Wiethe)

Annals of Otology, Rhinology & Laryngology, 1964
R F, DICKEY, S, DAVIS
openaire   +2 more sources

Advances in treatment for lipoid proteinosis (Urbach–Wiethe disease): a case report and systematic review

Clinical and Experimental Dermatology
Abstract Background Lipoid proteinosis (LP), also known as Urbach–Wiethe disease, is a rare autosomal recessive genodermatosis, caused by mutations in the ECM1 gene. This results in the deposition of periodic acid–Schiff (PAS)-positive, hyaline-like material on the skin, mucosae and internal organs.
Rocío C Bueno-Molina   +5 more
openaire   +2 more sources

Ultrastructural aspects of the skin in lipoid proteinosis (Urbach-Wiethe disease)

Anais Brasileiros De Dermatologia, 2021
Marilia Ogawa   +2 more
exaly  

Neurologic involvement in Urbach‐Wiethe's disease (lipoid proteinosis)

Neurology, 1971
F H, Newton   +3 more
openaire   +2 more sources

Pyoderma gangrenosum in a patient with lipoid proteinosis (Urbach–Wiethe disease)

Journal of the European Academy of Dermatology and Venereology, 2019
A.C. Pilz   +4 more
openaire   +1 more source

Lipoid proteinosis unveiled by oral mucosal lesions: a comprehensive analysis of 137 cases

Clinical Oral Investigations, 2016
Noam Yarom   +2 more
exaly  

Amygdalae Calcifications Associated with Disease Duration in Lipoid Proteinosis

Journal of Neuroimaging, 2006
Simone Appenzeller, Cendes Fernando
exaly  

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