Turner Syndrome

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dc.contributor.authorGupta, Ravinder K
dc.contributor.authorGupta, Ritu
dc.contributor.authorSharma, Sunil Dutt
dc.date.accessioned2016-02-01T07:04:08Z
dc.date.available2016-02-01T07:04:08Z
dc.date.issued2006-10
dc.description.abstractTurner Syndrome is one of the important chromosomal disorders characterised by loss (total or part) of sex chromosome. The manifestations being peripheral edema, short stature, extra skin fold, webbing of neck, renal and cardiovascular anomalies, sexual infantilism, learning disability etc. We present here a one month female baby who had classical features of Turner Syndrome. The karyotape analysis was consistent with the diagnosis.en_US
dc.identifier.citationGupta Ravinder K, Gupta Ritu, Sharma Sunil Dutt. Turner Syndrome. JK Science Journal of Medical Education and Research. 2006 Oct-Dec;8(4): 219-221en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/171353
dc.language.isoenen_US
dc.source.urihttps://www.jkscience.org/archive/vol8a/turner.pdfen_US
dc.subjectTurner Syndromeen_US
dc.subjectChromosomeen_US
dc.subjectPeripheral edemaen_US
dc.titleTurner Syndromeen_US
dc.typeArticleen_US
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