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Meckel-Gruber syndrome

dc.contributor.authorGAZIOGLU, N
dc.contributor.authorKUDAY, Cengiz
dc.contributor.authorERGINEL, A
dc.contributor.authorCENANI, A
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorILIKKAN, Barbaros
dc.contributor.authorVURAL, M
dc.contributor.authorSECKIN, MS
dc.contributor.authorAKPIR, E
dc.date.accessioned2021-03-05T14:48:33Z
dc.date.available2021-03-05T14:48:33Z
dc.date.issued1998
dc.identifier.citationGAZIOGLU N., VURAL M., SECKIN M., Tuysuz B., AKPIR E., KUDAY C., ILIKKAN B., ERGINEL A., CENANI A., "Meckel-Gruber syndrome", CHILDS NERVOUS SYSTEM, cilt.14, ss.142-145, 1998
dc.identifier.issn0256-7040
dc.identifier.otherav_b8f325f6-3656-40f6-b152-990fa815bf8e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/123062
dc.identifier.urihttps://doi.org/10.1007/s003810050198
dc.description.abstractMeckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, polydactyly and polycystic kidneys. This rare syndrome has been reported in the literature as incompatible with life. We present the case of a newborn afflicted with the clinical triad of Meckel-Gruber syndrome. Appropriate treatment instituted in our case led to a good early outcome.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectCERRAHİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.titleMeckel-Gruber syndrome
dc.typeMakale
dc.relation.journalCHILDS NERVOUS SYSTEM
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume14
dc.identifier.issue3
dc.identifier.startpage142
dc.identifier.endpage145
dc.contributor.firstauthorID9944


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