Publication:
A five month old girl with deletion in 5th chromosome: Cri du chat syndrome

dc.contributor.authorŞen, Tolga Altuğ
dc.contributor.authorMelek, Hamide
dc.contributor.authorKöken, Reflit
dc.contributor.buuauthorİmirzalioglu, Necat
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.
dc.date.accessioned2024-09-18T05:34:28Z
dc.date.available2024-09-18T05:34:28Z
dc.date.issued2008-09-01
dc.description.abstractThis five month-old girl was admitted to our clinic due to failure to thrive. On physical examination, her weight, length and head circumference was below the 3rd percentile, she had blond hair, facial dysmorphism and high arched palate. Pronounced hypotonia and motor retardation was present and high-pitched crying was striking. In echocardiographic examination, secundum type ASD and midtrabecular VSD without any important hemodynamic effect was present. In cranial MRI exmination, dilated 4th ventricles and delayed myelinisation in basal ganglia was detected. By the help of high resolution binding teqhnique, deletion in the short arm of the 5th chromosome was detected and diagnosis of Cri du Chat Syndrome was made.
dc.identifier.endpage88
dc.identifier.issn1304-9054
dc.identifier.issue2
dc.identifier.startpage86
dc.identifier.urihttps://hdl.handle.net/11452/44854
dc.identifier.volume6
dc.identifier.wos000422250300009
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherGalenos Yayincilik
dc.relation.journalGuncel Pediatri-journal Of Current Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCat cry
dc.subjectChromosome 5
dc.subjectDeletion
dc.subjectHypotonia
dc.subjectFailure to thrive
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectPediatrics
dc.titleA five month old girl with deletion in 5th chromosome: Cri du chat syndrome
dc.typeArticle
dspace.entity.typePublication

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