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dc.contributor.authorFarzannia, A
dc.contributor.authorShokouhi, G
dc.contributor.authorHadidchi, S
dc.date.accessioned2018-08-26T08:33:41Z
dc.date.available2018-08-26T08:33:41Z
dc.date.issued2003
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52460
dc.description.abstractAlkaptonuria is a rare metabolic disease caused by deficiency of homogentisic acid oxidase and characterized by bluish-black discoloration of cartilages and skin (ochronosis). The authors report the cases of three patients with lumbar disc herniation who underwent discectomy and in whom the nucleus pulposus was discovered to be black. Alkaptonuria was diagnosed after discectomy. Discal herniation requiring surgery is unusual in alkaptonuria, with only a few reports. The symptoms in the three patients disappeared after surgery and no symptoms were demonstrated on follow-up examination.
dc.language.isoEnglish
dc.relation.ispartofJournal of Neurosurgery
dc.subjectadult
dc.subjectalkaptonuria
dc.subjectarticle
dc.subjectcase report
dc.subjectclinical examination
dc.subjectclinical feature
dc.subjectcolor
dc.subjectcomputer assisted tomography
dc.subjectdisease course
dc.subjectfamily history
dc.subjectfemale
dc.subjectfollow up
dc.subjecthuman
dc.subjectintervertebral diskectomy
dc.subjectintraoperative period
dc.subjectlumbar disk hernia
dc.subjectmale
dc.subjectmyelography
dc.subjectneurologic examination
dc.subjectnuclear magnetic resonance imaging
dc.subjectnucleus pulposus
dc.subjectpathology
dc.subjectpostoperative period
dc.subjectpriority journal
dc.subjectsurgical technique
dc.subjecttreatment outcome
dc.subjecturinalysis
dc.subjectAdult
dc.subjectAlkaptonuria
dc.subjectDiskectomy
dc.subjectFemale
dc.subjectHumans
dc.subjectIntervertebral Disk Displacement
dc.subjectMale
dc.subjectOchronosis
dc.titleAlkaptonuria and lumbar disc herniation: Report of three cases
dc.typeArticle
dc.citation.volume98
dc.citation.issue1
dc.citation.spage87
dc.citation.epage89
dc.citation.indexScopus
dc.identifier.DOIDOI: https://doi.org/10.3171/spi.2003.98.1.0087


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