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BRIEF COMMUNICATION
Year : 2015  |  Volume : 63  |  Issue : 10  |  Page : 800-803

Bilateral congenital lacrimal fistulas in an adult as part of ectrodactyly-ectodermal dysplasia-clefting syndrome: A rare anomaly


1 Department of ENT, R. G. Kar Medical College, Kolkata, West Bengal, India
2 Department of ENT, Nilratan Sircar Medical College, Kolkata, West Bengal, India

Correspondence Address:
Dr. Debangshu Ghosh
Kalyan Nagar (Near K. G. School), P.O.-Kalyan Nagar, Via-Panshila, Dist.-24, Parganas (North), Kolkata - 700 112, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.171524

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Ectrodactyly-ectodermal dysplasia and clefting syndrome or "Lobster claw" deformity is a rare congenital anomaly that affects tissues of ectodermal and mesodermal origin. Nasolacrimal duct (NLD) obstruction with or without atresia of lacrimal passage is a common finding of such a syndrome. The authors report here even a rarer presentation of the syndrome which manifested as bilateral NLD obstruction and lacrimal fistula along with cleft lip and palate, syndactyly affecting all four limbs, mild mental retardation, otitis media, and sinusitis. Lacrimal duct obstruction and fistula were managed successfully with endoscopic dacryocystorhinostomy (DCR) which is a good alternative to lacrimal probing or open DCR in such a case.


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