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CASE REPORT
Year : 2014  |  Volume : 15  |  Issue : 3  |  Page : 130-132

A case of acro-dermato-ungual-lacrimal-tooth syndrome with chronic parotitis: A new association?


1 Department of Paediatrics, Lady Ridgeway Children's Hospital, Colombo, Sri Lanka
2 Department of Dermatology, Lady Ridgeway Children's Hospital, Colombo, Sri Lanka

Correspondence Address:
N Ginige
Department of Paediatrics, Lady Ridgeway Children's Hospital, Colombo
Sri Lanka
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2319-7250.143672

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Acro-dermato-ungual-lacrimal-tooth syndrome is characterized by ectrodactyly, syndactyly, nail dysplasia, hypoplasia of the breast and nipple, excessive freckling, lacrimal duct atresia, alopecia, primary hypodontia, and/or early loss of permanent teeth. It is a rare autosomal dominant disorder, which has been linked to mutation in the p63 gene. However unfortunately, the facilities to detect this mutation are not present in many centers. Five overlapping limb malformation syndromes have been described, including the ectrodactyly-ectodermal dysplasia-cleft syndrome .


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