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Lipoid proteinosis in two Iranian sisters: a case report and review of literature
IRCMJ-Iranian Red Crescent Medical Journal. 2011; 13 (4): 280-282
in English | IMEMR | ID: emr-110076
ABSTRACT
Lipoid proteinosis is a rare autosomal recessive disorder which may be seen within a family very occasionally. Herein, we report lipoid proteinosis in two sisters characterized by verrucous lesions and hoarseness of voice, dysphagia and multiple beaded papules along the margins of their eyelids, fissured lips and thick ferenulum
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Index: IMEMR (Eastern Mediterranean) Main subject: Review Literature as Topic / Eyelid Diseases / Lipoid Proteinosis of Urbach and Wiethe / Intellectual Disability Type of study: Case report Limits: Female / Humans Language: English Journal: Iran. Red Crescent Med. J. Year: 2011

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Index: IMEMR (Eastern Mediterranean) Main subject: Review Literature as Topic / Eyelid Diseases / Lipoid Proteinosis of Urbach and Wiethe / Intellectual Disability Type of study: Case report Limits: Female / Humans Language: English Journal: Iran. Red Crescent Med. J. Year: 2011