Lipoid proteinosis: Report of four siblings and brief review of the literature

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dc.contributor.author Nanda, A.
dc.contributor.author Alsaleh, Q.A.
dc.contributor.author Al-Sabah, H.
dc.contributor.author Ali, A.M.A.
dc.contributor.author Anim, J.T.
dc.date.accessioned 2013-06-25T20:38:51Z
dc.date.accessioned 2017-10-19T12:35:42Z
dc.date.available 2013-06-25T20:38:51Z
dc.date.available 2017-10-19T12:35:42Z
dc.date.issued 2001
dc.identifier.citation Nanda, A., Alsaleh, Q. A., Al-Sabah, H., Ali, A. M. A., & Anim, J. T. (2001). Lipoid proteinosis: Report of four siblings and brief review of the literature. Pediatric Dermatology, 18(1), 21-26. en_US
dc.identifier.issn 07368046
dc.identifier.uri http://197.255.68.203/handle/123456789/4138
dc.description.abstract Lipoid proteinosis (Urbach-Wiethe disease) is a rare autosomal recessive disorder associated with deposition of periodic acid-Schiff (PAS)-positive hyaline material in various tissues including skin, mucous membranes, and internal organs. A family is reported in which four siblings (two boys and two girls) born to nonconsanguineous parents had lipoid proteinosis. All had the characteristic hoarseness of voice and three had skin lesions. The diagnosis was confirmed by the presence of typical features on light and electron microscopy. en_US
dc.language.iso en en_US
dc.publisher Pediatric Dermatology en_US
dc.subject case report en_US
dc.subject lipoid proteinosis en_US
dc.title Lipoid proteinosis: Report of four siblings and brief review of the literature en_US
dc.type Article en_US


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