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Updated: Apr 23, 2026
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Separation of Mouse Embryonic Facial Ectoderm and Mesenchyme
Published on: April 12, 2013
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Ectrodactyly-ectodermal dysplasia-cleft lip and palate syndrome
Reema Sharma Dhar, Amitava Bora1
1Department of Pedodontics and Preventive Dentistry, Guru Nanak Institute of Dental Science and Research, Nilgunj Road, Panihati, Sodepur, Kolkata, West Bengal, India.
Journal of the Indian Society of Pedodontics and Preventive Dentistry
|September 19, 2014
Summary
Ectrodactyly-ectodermal dysplasia-cleft (EEC) syndrome, a rare disorder, presents with distinct physical anomalies. This case report details a child with EEC syndrome, highlighting its complex features and dental management.
Area of Science:
- Genetics and Developmental Biology
- Oral and Maxillofacial Surgery
- Pediatric Dentistry
Background:
- Ectrodactyly-ectodermal dysplasia-cleft (EEC) syndrome is an autosomal dominant disorder.
- It is characterized by the triad of ectrodactyly, ectodermal dysplasia, and facial clefting.
Observation:
- A rare case of EEC syndrome in a 4-year-old child is presented.
- The child exhibited ectrodermal dysplasia, cleft lip and palate, and ectrodactyly, along with other associated features.
Findings:
- The diagnosis of EEC syndrome was confirmed based on the clinical presentation.
- The report emphasizes the rarity of individuals presenting with all three major features of EEC syndrome.
Implications:
- This case highlights the importance of early diagnosis and a multidisciplinary approach for managing EEC syndrome.
- The crucial role of dentists in the comprehensive treatment of patients with EEC syndrome is underscored.
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