Cutis laxa syndrome: A case report

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Abstract

Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal recessive and x-linked recessive patterns have been described in the inherited forms. Acquired forms of this disease have been associated with a previous inflammatory skin disorder (urticaria…). The characteristic symptomatological pattern is resulting from paucity of elastic fibers. We report an 18 months old baby boy with a congenital cutis laxa. He was admitted in pediatric unit for respiratory disorders. The diagnosis of CL syndrome is based on clinical assessment of typical skin features and the associated extracutaneous finding.

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Hbibi, M., Abourazzak, S., Idrissi, M., Chaouki, S., Atmani, S., & Hida, M. (2015). Cutis laxa syndrome: A case report. Pan African Medical Journal, 20. https://doi.org/10.11604/pamj.2015.20.3.5878

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