ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT-LIP SYNDROME - CASE-REPORT

Authors
SENO H YANAI A SUGINO H INOUE M TAKEI T MIYAKE I
Citation
H. Seno et al., ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT-LIP SYNDROME - CASE-REPORT, Scandinavian journal of plastic and reconstructive surgery and hand surgery, 30(3), 1996, pp. 227-230
Citations number
22
Categorie Soggetti
Surgery
Journal title
Scandinavian journal of plastic and reconstructive surgery and hand surgery → ACNP
ISSN journal
02844311
Volume
30
Issue
3
Year of publication
1996
Pages
227 - 230
Database
ISI
SICI code
0284-4311(1996)30:3<227:EEDACS>2.0.ZU;2-2
Abstract
We describe five sporadic cases of the EEC syndrome (ectrodactyly, ect odermal dysplasia, and cleft lip). There are only a few reports of the syndrome being inherited in Japan. Two of the five patients had genit ourinary anomalies and one mental retardation. Four of the five patien ts had clefts in the primary and secondary palate. All had deformities of the hands, polydactyly, syndactyly, and camptodactyly. Syndactyly could be a component of the syndrome.