Bilateral Congenital Entropion with Cutis Laxa
Article first published online: 11 FEB 2014
© 2014 Wiley Periodicals, Inc.
Volume 31, Issue 3, pages e82–e84, May/June 2014
How to Cite
Al-Faky, Y. H., Salih, M. A., Mubarak, M. and Al-Rikabi, A. C. (2014), Bilateral Congenital Entropion with Cutis Laxa. Pediatric Dermatology, 31: e82–e84. doi: 10.1111/pde.12255
- Issue published online: 24 APR 2014
- Article first published online: 11 FEB 2014
Cutis laxa is a rare connective tissue disorder characterized by redundant and pendulous skin due to a defect in the elastic fiber network. Two cases of entropion associated with cutis laxa have been reported, although entropion was due to elongation of the anterior lamella or horizontal lid laxity. Thorough systemic and ophthalmic evaluations were performed, as well as chart review for the perinatal period. Surgical correction of entropion through posterior tarsotomy was done. An infant boy with dysmorphic features and furrowing of the skin of the entire body without hyperelasticity, which is typical for cutis laxa, presented with bilateral congenital entropion. We report here for the first time a different etiology of congenital entropion with cutis laxa: the eyelashes were abnormally directed due to the unusual location of their roots, which were embedded within the tarsus. Moreover, this is the only case of cutis laxa with congenital entropion involving both upper and lower eyelids. Congenital entropion can be associated with cutis laxa. Although elongation of the anterior lamella and horizontal lid laxity predispose to such an entropion, abnormal location of the roots of the eyelashes might be encountered and marginal eyelid rotation surgery is indicated.