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Rare 48, XYYY syndrome: case report and review of the literature

dc.contributor.authorAbedi, M
dc.contributor.authorSalmaninejad, A
dc.contributor.authorSakhinia, E
dc.date.accessioned2018-08-26T07:13:00Z
dc.date.available2018-08-26T07:13:00Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44857
dc.description.abstract48, XYYY syndrome is a rare condition. A male with 32-year-old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi-Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity of the joints, likewise mental health problems were obvious.
dc.language.isoEnglish
dc.relation.ispartofCLINICAL CASE REPORTS
dc.subject48, XYYY syndrome
dc.subjectchromosomal abnormality
dc.subjectcytogenetic
dc.subjectQF-PCR
dc.subjectsex chromosome
dc.titleRare 48, XYYY syndrome: case report and review of the literature
dc.typeReview
dc.citation.volume6
dc.citation.issue1
dc.citation.spage179
dc.citation.epage184
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1002/ccr3.1311


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