Ectrodactyly, Ectodermal Dysplasia, Cleft Lip, and Palate (EEC Syndrome) with Tetralogy of Fallot: A Very Rare Combination
Author:
Publisher
Frontiers Media SA
Subject
Pediatrics, Perinatology and Child Health
Reference36 articles.
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2. p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities;Yang;Mol Cell,1998
3. The p63 gene in EEC and other syndromes;Brunner;J Med Genet,2002
4. The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization;Fukushima;Clin Genet,1993
5. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3;Qumsiyeh;Clin Genet,1992
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1. Peripheral giant cell granuloma in a child with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome: a case report;BMC Oral Health;2024-08-13
2. The Prevalence of Dental Malocclusions among Cleft Lip and Palate Patients;Journal of Indian Academy of Oral Medicine and Radiology;2024
3. Ocular Manifestations in Patients Affected by p63-Associated Disorders: Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) and Ankyloblepharon-Ectodermal Defects-Cleft Lip Palate (AEC) Syndromes;Journal of Clinical Medicine;2023-11-28
4. A newborn with ectrodactyly, tetralogy of Fallot, esophageal atresia, hypospadias and TP63 gene mutation: A new type of EEC Syndrome?;Journal of Neonatal-Perinatal Medicine;2023-06-27
5. Overlap between EEC and AEC syndrome and immunodeficiency in a preterm infant with a TP63 variant;European Journal of Medical Genetics;2023-05
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