Results 141 to 150 of about 1,156 (180)

Spontaneous intracerebral hemorrhage in Urbach-Wiethe disease

Neurology, 2012
A 39-year-old woman born from consanguineous parents was referred to our department for a second opinion regarding a left lenticular nucleus hemorrhage resulting in right hemiparesis, which occurred 1 year before in absence of history of hypertension, diabetes, smoking, or substance abuse ...
Maria Josè, Messina, Graziamaria, Nuzzaco, Alessandra, Barbieri, Marina, Scarlato, Simonetta, Gerevini, Vittorio, Martinelli, Giancarlo, Comi, Maria, Sessa   +7 more
openaire   +2 more sources

OC12
Lipoid proteinosis (Urbach‐Wiethe disease)

Oral Diseases, 2006
Lipoid 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, Ö Dog˘an Onur, V Olgaç, A Balik, B Batur   +4 more
openaire   +1 more source

Marathon of eponyms: 21 Urbach‐Wiethe disease (Lipoid proteinosis)

Oral Diseases, 2011
Oral 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
openaire   +2 more sources

[Urbach-Wiethe disease/lipoidproteinosis].

Acta medica portuguesa, 1999
The authors present a case of Urbach-Wiethe's disease (lipoid proteinosis), a rare autosomal recessive disorder, in a 49-year-old female patient with pathognomonic cranial radiological findings demonstrated by radiology and computed tomography. The rarity of this pathology made radiological diagnosis difficult.
R, Maia, L, Teixeira, J, Drago
openaire   +1 more source

[Urbach-Wiethe disease. Apropos of 2 cases].

Annales d'oto-laryngologie et de chirurgie cervico faciale : bulletin de la Societe d'oto-laryngologie des hopitaux de Paris, 1986
The Urbach-Wiethe disease is a rare condition, where a hyaline substance of an unknown biochemical nature is accumulated in both teguments and mucous membranes. It has an autosomic and recessive genetic transmission. Cutaneous and mucous lesions (especially on the upper digestive tract) are described, insisting about the laryngeal location and the ...
M, Wayoff, M, Weber, C, Pinelli, P, Maxant, C, Moret   +4 more
openaire   +1 more source

Urbach — Wiethe disease — life without fear (clinical case)

Russian Journal of Clinical Dermatology and Venereology
Urbach — Wiethe disease (lipoid proteinosis) is a rare genetic dermatosis caused by mutation in ECM1 gene on chromosome 1, that encodes extracellular matrix protein 1. This disease can affect the skin, upper respiratory tract, brain, less often — other visceral organs.
A.Sh. Aliev, E.V. Koldarova, B.I. Mukhamedov, M.N. Solmetova   +3 more
openaire   +1 more source

Urbach-Wiethe Disease(Lipoid Proteinosis)

Pediatric Neurosurgery, 1998
C C, Staut, T P, Naidich
openaire   +2 more sources

Urbach-Wiethe Disease

2009
Gudrun Rappold, John-John B. Schnog, Victor E. A. Gerdes, Yvonne G. Weber, Jose M. Serratosa, Anna-Elina Lehesjoki, Alessandra Baumer, André B. P. Kuilenburg, Albert H. Gennip*, David C. Rees, Lynette D. Fairbanks, H. Anne Simmonds, Albrecht Hesse, Albrecht Hesse, Diana J. Zimmermann, Gerd E. Von Unruh, Bernd Hoppe, Roswitha Siener, Albrecht Hesse, Naim M. Maalouf, MaryAnn Cameron, Khashayar Sakhaee, Alexander K. C. Leung, Susan Kupka, Markus Pfister, Nikolaos E. Bechrakis, Henry J. Kaplan, Hui Shao, Deming Sun   +28 more
openaire   +1 more source

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, SOYUER, Işın, KÜLAHCI, İsmail, TATLIŞEN, Nursen   +3 more
openaire   +1 more source

[Urbach-Wiethe disease].

Bulletin de la Societe francaise de dermatologie et de syphiligraphie, 1971
E, Hadida, J, Civatte, J, Sayag
openaire   +3 more sources