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dc.contributor.authorFarzannia, A
dc.contributor.authorShokouhi, G
dc.contributor.authorHadidchi, S
dc.date.accessioned2018-08-26T06:34:33Z
dc.date.available2018-08-26T06:34:33Z
dc.date.issued2003
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44012
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.subjectDiskectomy
dc.subjectFemale
dc.subjectHumans
dc.subjectIntervertebral Disc Displacement
dc.subjectMale
dc.subjectOchronosis
dc.titleAlkaptonuria and lumbar disc herniation. Report of three cases.
dc.typearticle
dc.citation.volume98
dc.citation.issue1 Suppl
dc.citation.spage87
dc.citation.epage9
dc.citation.indexPubmed


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