Acrania: Two case reports with prenatal ultrasound results

dc.contributor.authorKoç, Mustafa
dc.contributor.authorAkbaş, Gökhan
dc.date.accessioned2026-08-12T16:15:45Z
dc.date.issued2008
dc.departmentFırat Üniversitesi
dc.description.abstractAcrania is a rare congenital anomaly and characterized by partial or complete absence of the calvarium with abnormal brain tissue development. The pathogenesis of acrania is unknown and differential diagnosis should be searched to rule out other similer conditions to anencephaly and acalvaria. Diagnosis of cranial bone defects can be established by ultrasonography in the first trimester of pregnancy. We report two cases, diagnosed prenatally by ultrasonography, one with isolated acrania and the other one associated with meningocele.
dc.identifier.endpage110
dc.identifier.issn1300-199X
dc.identifier.issue2
dc.identifier.scopus2-s2.0-46749135600
dc.identifier.scopusqualityN/A
dc.identifier.startpage107
dc.identifier.urihttps://hdl.handle.net/11508/43869
dc.identifier.volume30
dc.indekslendigikaynakScopus
dc.language.isoen
dc.relation.ispartofErciyes Tip Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20260511
dc.subjectAcrania; Prenatal diagnosis; Ultrasonography, prenatal
dc.titleAcrania: Two case reports with prenatal ultrasound results
dc.typeArticle

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