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Lower eyelid involvement occurs in 6% of patients with discoid lupus erythematosus (DLE). Eyelid lesions are rarely the initial manifestation of DLE. We describe a 25-year-old woman presenting with… Expand
Classic lamellar ichthyosis is a rare, autosomal recessive, genetically heterogeneous skin disease caused by mutations in the transglutaminase 1 gene. Pseudoainhum is characterized by the appearance… Expand
Autosomal recessive primary ichthyosis (ARPI) is a rare, genetically heterogeneous skin disease. Several loci of responsible genes have been identified, including 14q11, which controls… Expand
Background Anti-tumour necrosis factor alpha are a well-documented class of disease-modifying therapy for inflammatory bowel diseases, including Crohn's disease and ulcerative colitis. The… Expand
Il controllo dell’iperfosfatemia e ancora oggi uno degli aspetti piu critici fra i disordini del metabolismo minerale nel paziente uremico in dialisi: infatti oltre ad essere uno dei meccanismi… Expand