Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4138
Title: Lipoid proteinosis: Report of four siblings and brief review of the literature
Authors: Nanda, A.
Alsaleh, Q.A.
Al-Sabah, H.
Ali, A.M.A.
Anim, J.T.
Keywords: case report
lipoid proteinosis
Issue Date: 2001
Publisher: Pediatric Dermatology
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.
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.
URI: http://hdl.handle.net/123456789/4138
ISSN: 07368046
Appears in Collections:Department of Pathology 9

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