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dc.contributor.authorBarzegar, M
dc.contributor.authorFayyazie, A
dc.contributor.authorGasemie, B
dc.contributor.authorShoja, MAM
dc.date.accessioned2018-08-26T08:28:39Z
dc.date.available2018-08-26T08:28:39Z
dc.date.issued2007
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51576
dc.description.abstractIntroduction: Menkes disease is a rare X-linked recessive disorder of copper metabolism. It is characterized by progressive cerebral degeneration with psychomotor deterioration, hypothermia, seizures and characteristic facial appearance with hair abnormalities. Case Presentation: We report on two cases of classical Menkes disease with typical history., (progressive psychomotor deterioration and seizures}, clinical manifestations (cherubic appearance, with brittle, scattered and hypopigmented scalp hairs), and progression. Light microscopic examination of the hair demonstrated the pili torti pattern. The low serum copper content and ceruloplasmin confirmed the diagnosis. Conclusion: Menkes disease is an under-diagnosed entity, being familiar with its manifestation and maintaining high index of suspicion are necessary for early diagnosis.
dc.language.isoEnglish
dc.relation.ispartofIRANIAN JOURNAL OF PEDIATRICS
dc.subjectMenkes disease
dc.subjectcopper metabolism
dc.subjectepilepsy
dc.subjectpili torti
dc.subjectcerebral degeneration
dc.titleMenkes disease: Report of two cases
dc.typeArticle
dc.citation.volume17
dc.citation.issue4
dc.citation.spage388
dc.citation.epage392
dc.citation.indexWeb of science


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