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Artigo em Inglês | IMSEAR | ID: sea-171149

RESUMO

Lamellar ichthyosis is a rare, autosomal recessive, genetically heterogeneous skin disorder caused by mutations in the transglutaminase-1 gene. Eye abnormalities include bilateral ectropion of lower lids, chronic blepharitis and rarely cataract. A case of lamellar ichthyosis with bilateral lower lid ectropion and bilateral mature cataract is hereby presented for its rarity.

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