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EEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): A clinical case report

dc.contributor.authorUlukapi, I
dc.contributor.authorYalcin, S
dc.contributor.authorBilgin, T
dc.date.accessioned2021-03-03T10:18:49Z
dc.date.available2021-03-03T10:18:49Z
dc.identifier.citationUlukapi I., Bilgin T., Yalcin S., "EEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): A clinical case report", JOURNAL OF DENTISTRY FOR CHILDREN, cilt.68, ss.350-353, 2001
dc.identifier.issn0022-0353
dc.identifier.othervv_1032021
dc.identifier.otherav_21ece739-4367-41dc-b6b5-952974ec5048
dc.identifier.urihttp://hdl.handle.net/20.500.12627/27824
dc.description.abstractThe EEC syndrome (ectrodactyly-ectodermal dysphasia-clefting) is defined as a multiple congenital anomaly syndrome characterized by ectodermal dysplasia, distal limb anomaly; cleft lip/palate, and lacri man duct anomalies. This case report reviews and presents clinical symptoms and treatment of the EEC syndrome.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectDiş Hekimliği
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.titleEEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): A clinical case report
dc.typeMakale
dc.relation.journalJOURNAL OF DENTISTRY FOR CHILDREN
dc.contributor.department, ,
dc.identifier.volume68
dc.identifier.startpage350
dc.identifier.endpage353
dc.contributor.firstauthorID162812


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