| CASE REPORT |
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| Year : 2021 | Volume
: 9
| Issue : 3 | Page : 202-205 |
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Ectrodactyly–ectodermal dysplasia–clefting syndrome
Khooshbu Gayen, Anisha Bag, Supreet Shirolkar, Rajib Sikdar, Santanu Mukhopadhyay, Subir Sarkar
Department of Pedodontics and Preventive Dentistry, Dr. R Ahmed Dental College and Hospital, Kolkata, West Bengal, India
Correspondence Address:
Dr. Supreet Shirolkar
Department of Pedodontics 2C, Dr. R. Ahmed Dental College and Hospital, Kolkata - 700 014, West Bengal
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/njecp.njecp_19_21
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Ectrodactyly–ectodermal dysplasia–clefting (EEC) syndrome is a rare hereditary congenital defect characterized by a triad of disorders such as ectodermal dysplasia, malformed extremities, and cleft lip and/or palate. We report the case of a 3-month-old girl child with clinical signs of EEC syndrome and offer valuable information into current knowledge about this syndrome. The symptoms of EEC display diversity in both extension and expression. Early diagnosis and management of clinical manifestations associated with this syndrome presents a unique challenge due to the paucity of documents in the literature.
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