Lipoid Proteinosis Of Urbach And Wiethe
Mostrando 1-6 de 6 artigos, teses e dissertações.
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1. Assessment of dynamic thiol-disulfide homeostasis in patients with lipoid proteinosis (Urbach-Wiethe syndrome)
SUMMARY OBJECTIVE: Lipoid proteinosis is a rare autosomal recessive genetic dermatological disease that occurs due to the accumulation of hyaline material in the skin and mucous membranes. This study aimed to investigate whether dynamic thiol-disulfide homeostasis is a new marker of oxidative stress in patients suffering from lipoid proteinosis. METHODS: T
Revista da Associação Médica Brasileira. Publicado em: 2022
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2. Is it always blepharitis? Urbach-Wiethe syndrome (lipoid proteinosis)
RESUMO Uma menina de 12 anos apresentava restos crostosos e caspa recorrente na base de ambos os cílios, apesar de ter completado diferentes tratamentos médicos. Ela tinha uma voz rouca desde a infância. No exame do segmento anterior dos olhos, encontramos pápulas amarelo-esbranquiçadas nas margens das pálpebras. Um otorrinolaringologista detectou múl
Arq. Bras. Oftalmol.. Publicado em: 25/03/2019
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3. Mucous-cutaneuos hyalinosis : the clinical and histocompatibility antigens study / Hialinose cutaneo-mucosa : estudo clinico e das especificidades HLA
A hialinose cutâneo-mucosa (HCM) é uma dermatose autossômica recessiva rara, congênita, de aparecimento precoce na infância. Caracteriza-se por deposição de material hialino, que se acumula na pele e mucosas. Foram descritos 258 casos na literatura mundial e no Brasil, doze casos. A HCM apresenta aumento da expressão do colágeno tipo IV e V e reduç
Publicado em: 2008
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4. Corectopia and lipoid proteinosis.
Lipoid proteinosis (Urbach-Wiethe disease) is a rare autosomal recessive disorder associated with deposition of hyalinised material in the skin, mucous membrane, and brain. Corectopia has not been described in this disorder. A case is presented of lipoid proteinosis with bilateral corectopia.
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5. Lipoid proteinosis (Urbach-Wiethe syndrome).
A Jewish-Iranian family suffered from lipoid proteinosis. The 8 affected siblings were from consanguineous matings and presented a wide range of phenotypic expressions. Minimal manifestations in 2 heterozygote carriers and the possibility of autosomal recessive inheritance are discussed.
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6. A case of hyalinosis cutis et mucosae (lipoid proteinosis of Urbach and Wiethe) with common ancestors in four remote generations.
We report a case of hyalinosis cutis et mucosae, a rare disorder of hyalin deposition in skin and mucous membranes, in a 27-year-old male, whose coefficient of inbreeding was 0-0106 due to seven common ancestors, including an aunt of an early American president, in the eight preceding generations.