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

dc.contributor.author	Ulukapi, I
dc.contributor.author	Yalcin, S
dc.contributor.author	Bilgin, T
dc.date.accessioned	2021-03-03T10:18:49Z
dc.date.available	2021-03-03T10:18:49Z
dc.identifier.citation	Ulukapi 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.issn	0022-0353
dc.identifier.other	vv_1032021
dc.identifier.other	av_21ece739-4367-41dc-b6b5-952974ec5048
dc.identifier.uri	http://hdl.handle.net/20.500.12627/27824
dc.description.abstract	The 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.iso	eng
dc.subject	Dahili Tıp Bilimleri
dc.subject	Çocuk Sağlığı ve Hastalıkları
dc.subject	Diş Hekimliği
dc.subject	Tıp
dc.subject	Sağlık Bilimleri
dc.subject	PEDİATRİ
dc.subject	Klinik Tıp (MED)
dc.subject	Klinik Tıp
dc.subject	DİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.title	EEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): A clinical case report
dc.type	Makale
dc.relation.journal	JOURNAL OF DENTISTRY FOR CHILDREN
dc.contributor.department	, ,
dc.identifier.volume	68
dc.identifier.startpage	350
dc.identifier.endpage	353
dc.contributor.firstauthorID	162812

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