Sirenomelia: A Rare Entity

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dc.contributor.authorGupta, Sapna
dc.contributor.authorMehta, Anil
dc.contributor.authorSharma, Belu
dc.contributor.authorGupta, Nirupam
dc.contributor.authorLamba, Jyotsana
dc.date.accessioned2016-02-08T04:56:08Z
dc.date.available2016-02-08T04:56:08Z
dc.date.issued2011-01
dc.description.abstractSirenomelia also called as Mermaid Syndrome, is a rare congenital malformation of uncertain aetiology. It is characterised by fusion of the lower limbs and commonly associated with severe urogenital and gastrointestinal malformation. It should be suspected in antenatal period in cases presenting with severe oligohydramnios and intra-uterine growth retardation. Here, we report a case of sirenomelia in a 26th weeks foetus.en_US
dc.identifier.citationGupta Sapna, Mehta Anil, Sharma Belu, Gupta Nirupam, Lamba Jyotsana. Sirenomelia: A Rare Entity. JK Science Journal of Medical Education and Research. 2011 Jan-Mar; 13(1): 29-30en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/172007
dc.language.isoenen_US
dc.source.urihttps://www.jkscience.org/archive/volume131/Sirenomelia%20A%20Rare%20Entity.pdfen_US
dc.subjectSirenomeliaen_US
dc.subjectCaudal Regression Syndromeen_US
dc.titleSirenomelia: A Rare Entityen_US
dc.typeArticleen_US
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