Results 91 to 100 of about 332 (125)
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Orbit, 2011
Lipoid proteinosis (LP) or Urbach-Wiethe disease is a recessively inherited disorder not usually seen by ophthalmologists. It is characterized by non-inflammatory, persistent papules on the skin and mucous membranes. The first clinical manifestation of LP is usually progressive hoarseness.
Miquel, Callizo +5 more
exaly +3 more sources
Lipoid proteinosis (LP) or Urbach-Wiethe disease is a recessively inherited disorder not usually seen by ophthalmologists. It is characterized by non-inflammatory, persistent papules on the skin and mucous membranes. The first clinical manifestation of LP is usually progressive hoarseness.
Miquel, Callizo +5 more
exaly +3 more sources
LIPOID PROTEINOSIS: URBACH—WIETHE DISEASE
British Journal of Dermatology, 1976A Rook
exaly +3 more sources
Lipoid Proteinosis (Urbach-Wiethe's Disease)
JAMA - Journal of the American Medical Association, 1963exaly +2 more sources
Lipoid Proteinosis (Urbach-Wiethe Disease)
Ophthalmologica, 1999The aim of this study has been to assess the clinical presentation and biochemical profile of lipoid proteinosis within a defined pedigree. Glycoprotein analysis was compared to normal values in an attempt to define a biochemical phenotype. Six affected family members were identified with variable degrees of disease expression.
Costagliola C +5 more
openaire +6 more sources
Lipoid Proteinosis (of Urbach-Wiethe)
Archives of Ophthalmology, 1963Introduction Lipoid proteinosis is a rare disease of skin and mucous membranes. Characteristic lesions of the eyelid occur, but we have found only one case in the ophthalmic literature.1Although the earliest clinical report appeared in 1908, it was not until Urbach and Wiethe's 1929 article that the disease was extensively studied.
J. F. MUIRHEAD, P. JACKSON
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OC12 Lipoid proteinosis (Urbach‐Wiethe disease)
Oral Diseases, 2006Lipoid proteinosis (LP), also known as Urbach‐Wiethe disease is a rare, autosomal recessive disorder associated with deposition of acid‐Schiff (PAS)‐positive hyaline‐like material in various tissues including skin, mucosal membranes and internal organs. The aetiology of LP is currently unknown.
B Kurtuluş +4 more
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Marathon of eponyms: 21 Urbach‐Wiethe disease (Lipoid proteinosis)
Oral Diseases, 2011Oral Diseases (2011) 17, 729–730The use of eponyms has long been contentious, but many remain in common use, as discussed elsewhere (Editorial: Oral Diseases. 2009: 15; 185). The use of eponyms in diseases of the head and neck is found mainly in specialties dealing with medically compromised individuals (paediatric dentistry, special care dentistry ...
C, Scully, J, Langdon, J, Evans
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[Lipoid proteinosis (Urbach-Wiethe's Disease)].
Kulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat, 2016A 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.
Hatice, Karaman +3 more
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[Urbach-Wiethe disease (lipoid proteinosis) with neurological involvement].
Annales de dermatologie et de venereologie, 2007Lipoid proteinosis is a rare autosomal recessive disease that has recently been shown to result from mutations in the ECM1 gene. Some cases are associated with a more severe mucocutaneous phenotype.We report the case of a 38-year-old woman who had clinical and histological skin features typical of Urbach-Wiethe disease.
A, Maruani +5 more
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