Kidney stone and urinary bladder telangiectasia in a patient with TAR syndrome

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dc.contributor.authorAkil I.
dc.contributor.authorGözmen S.
dc.contributor.authorYilmaz Ö.
dc.contributor.authorTaneli C.
dc.date.accessioned2024-07-22T08:22:04Z
dc.date.available2024-07-22T08:22:04Z
dc.date.issued2008
dc.description.abstractTAR syndrome is a congenital malformation syndrome characterized by bilateral absence of the radius and thrombocytopenia. The known urinary anomalies are duplex ureter, dilatation of renal pelvis, horseshoe kidney and functional problems like vesicoureteral reflux and pyelonephritis. In this report of a case with TAR syndrome, a kidney stone and bladder telangiectasia were found coincidentally during the investigation of hematuria. TAR syndrome is discussed in the light of the medical literature. To our knowledge, no case has been reported demonstrating nephrolithiasis and bladder telangiectasia in TAR patients.
dc.identifier.issn00414301
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/18911
dc.language.isoEnglish
dc.subjectChild
dc.subjectCystoscopy
dc.subjectDiagnosis, Differential
dc.subjectHumans
dc.subjectKidney Calculi
dc.subjectMale
dc.subjectRadius
dc.subjectSyndrome
dc.subjectTelangiectasis
dc.subjectThrombocytopenia
dc.subjectUrinary Bladder Diseases
dc.subjectarticle
dc.subjectcase report
dc.subjectchild
dc.subjectcomputer assisted tomography
dc.subjectdiet restriction
dc.subjectechography
dc.subjecthematologic disease
dc.subjecthematuria
dc.subjecthuman
dc.subjectincidental finding
dc.subjectmale
dc.subjectnephrolithiasis
dc.subjectschool child
dc.subjectskeleton malformation
dc.subjecttelangiectasia
dc.subjectthrombocytopenia and absence of the radius syndrome
dc.subjectureter stone
dc.subjectbladder disease
dc.subjectcongenital malformation
dc.subjectcystoscopy
dc.subjectdifferential diagnosis
dc.subjectnephrolithiasis
dc.subjectradius
dc.subjectsyndrome
dc.subjecttelangiectasia
dc.subjectthrombocytopenia
dc.titleKidney stone and urinary bladder telangiectasia in a patient with TAR syndrome
dc.typeArticle

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