Edward’s syndrome with a novel karyotype.

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dc.contributor.authorPatra, S
dc.contributor.authorGarg, A
dc.contributor.authorGulati, A
dc.contributor.authorKrishnamurthy, S
dc.contributor.authorAneja, S
dc.date.accessioned2015-12-07T09:23:38Z
dc.date.available2015-12-07T09:23:38Z
dc.date.issued2011
dc.description.abstractEdward’s syndrome was first described as a clinical entity in 1960 as a disorder of trisomy 18 (47 XX/XY; + 18) in babies with particular pattern of malformations. The Karyotype found in our case was (47 XX + 18 add (22) (p13) which has not been published so far in the literature. The less common findings noted in the baby were rocker bottom feet, syndactyly of 2nd and 3rd toes, microcephaly and corneal opacities. Though we didn’t find any significant association between phenotypic ranges with genotypic variation in literature, but further research is needed for it. We are reporting this case as the genotype is found to be novel.en_US
dc.identifier.citationPatra S, Garg A, Gulati A, Krishnamurthy S, Aneja S. Edward’s syndrome with a novel karyotype. Bangladesh Journal of Medical Science. 2011; 10(3): 211-212.en_US
dc.identifier.issn2223-4721
dc.identifier.issn2076-0299
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/167356
dc.language.isoenen_US
dc.source.urihttps://www.banglajol.info/index.php/BJMS/article/view/8368en_US
dc.subjectEdward’s syndromeen_US
dc.subjectkaryotypeen_US
dc.subjectneonateen_US
dc.titleEdward’s syndrome with a novel karyotype.en_US
dc.typeArticleen_US
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