Congenital midline cervical cleft: A rare embryo pathogenic disorder

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dc.contributor.authorGenç A.
dc.contributor.authorTaneli C.
dc.contributor.authorArslan O.A.
dc.contributor.authorDaǧlar Z.
dc.contributor.authorMir E.
dc.date.accessioned2024-07-22T08:25:12Z
dc.date.available2024-07-22T08:25:12Z
dc.date.issued2002
dc.description.abstractCongenital midline cervical cleft (CMCC) is a rare disorder of the ventral neck. The cleft consists of an epithelium-covered, longitudinal central depression with a protuberance at the cervical end. The adjacent skin is tethered by scar tissue forming a depression, which ends in a blind sinus at the caudal end. Although a variety of embryological mechanisms are proposed, its etiology is obscure. Up to the present time, fewer than 50 cases have been reported in the English literature. CMCC can be seen in association with several midline anomalies related to the branchial arches, including median cleft of the lower lip and mandible, and hypoplasia or absence of other midline neck structures. We present a 36-day-old boy with CMCC to illustrate its clinical presentation and the result at 24 months postoperatively. © Springer-Verlag 2002.
dc.identifier.DOI-ID10.1007/s00238-001-0336-6
dc.identifier.issn0930343X
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/20317
dc.language.isoEnglish
dc.subjectarticle
dc.subjectcase report
dc.subjectcleft lip
dc.subjectclinical feature
dc.subjectcongenital midline cervical cleft
dc.subjectdevelopmental disorder
dc.subjectembryology
dc.subjectepithelium
dc.subjecthuman
dc.subjecthypoplasia
dc.subjectmale
dc.subjectmandible
dc.subjectnewborn
dc.subjectpostoperative period
dc.subjectpriority journal
dc.subjectscar
dc.subjectskin
dc.titleCongenital midline cervical cleft: A rare embryo pathogenic disorder
dc.typeArticle

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