Ocular manifestations in lipoid proteinosis: A rare clinical entity

Autor: Sumana J Kamath, HimaBindu Marthala, BinduMadhavi Manapragada

Publikováno v: Indian Journal of Ophthalmology, Vol 63, Iss 10, Pp 793-795 (2015)

Lipoid proteinosis is a rare autosomal recessive genodermatosis with abnormal lipid protein complexes deposition in different parts of the body, especially in the skin and mucus membranes of the upper aerodigestive tract. Though ocular involvement in

Externí odkaz: https://doaj.org/article/662b289d308d4a698ba7dd38ce5ad712

Amygdala Lesions Reduce Anxiety-like Behavior in a Human Benzodiazepine-Sensitive Approach–Avoidance Conflict Test

Autor: Korn, Christoph W., Vunder, Johanna, Miró, Júlia, Fuentemilla, Lluís, Hurlemann, Rene, Bach, Dominik R.

Publikováno v: Biological Psychiatry

Background Rodent approach–avoidance conflict tests are common preclinical models of human anxiety disorder. Their translational validity mainly rests on the observation that anxiolytic drugs reduce rodent anxiety-like behavior. Here, we capitalize

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1262af966fe0c87450a8be7fe182541e
http://europepmc.org/articles/PMC5598543

É sempre blefarite? Síndrome de Urbach-Wiethe (proteinose lipóide)

Autor: Bahar Gunes, Remzi Karadag, Bengü Çobanoğlu Şimşek, Lokman Uzun, Ayse Serap Karadag

Publikováno v: Arquivos Brasileiros de Oftalmologia, Iss 0 (2019)
Arquivos Brasileiros de Oftalmologia, Volume: 82, Issue: 3, Pages: 242-244, Published: 25 MAR 2019
Arquivos Brasileiros de Oftalmologia, Issue: ahead, Published: 25 MAR 2019

A 12-year-old girl presented with recurrent crusty debris and dandruff at the base of both eyelashes despite having completed different medical treatments. She had had a hoarse voice since her early childhood. Upon anterior segment examination of the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21c1cfa4c87c5878fbd5d5fa7a70479b
https://doi.org/10.5935/0004-2749.20190051

Urbach-Wiethe syndrome

Autor: Jyoti Ranjan Parida, Vikas Agarwal, Durga Prasanna Misra

A 14-year-old girl was referred for skin tightening in the fingers. She did not have Raynaud's phenomenon, gastroesophageal reflux disease or other systemic symptoms. She had had a hoarse voice since birth and was developmentally normal. She was born

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6caa559c91f3214fcd992eda31068681
https://europepmc.org/articles/PMC4567717/

Belastungsabhängige Dysphonie, rezidivierende Pleuropneumonie und supraglottische Raumforderung

Autor: K. Jahn, H.-J. Straehler-Pohl, G. Schade, H.-P. Fischer

Publikováno v: HNO. 58:931-933

Das Urbach-Wiethe-Syndrom (Hyalinosis cutis et mucosae) ist eine Erkrankung mit autosomal-rezessivem Erbgang. Diese manifestiert sich oft mit typischen Symptomen wie Hautlasionen (v. a. im Bereich des Gesichts und des Halses), Dyspnoe und Maldigestio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::17415b5205f774a2d405a2c532f50b38
https://doi.org/10.1007/s00106-010-2119-5