Pseudotrisomy 13 syndrome : A case report.

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dc.contributor.authorVejabhuti, Choladda
dc.contributor.authorChuangsuwanich, Tuenjai
dc.contributor.authorSangruchi, Tumtip
dc.contributor.authorLimwongse, Chanin
dc.contributor.authorBotpibul, Suchatree
dc.contributor.authorKanokpongsakdi, Sujin
dc.date.accessioned2012-02-22T04:34:21Z
dc.date.available2012-02-22T04:34:21Z
dc.date.issued2003-07
dc.description.abstractWe report on a male baby with microcephaly, holoprosencephaly of alobar type with sigle ventricle, cyclopia, proboscis, poorly developed testes, and clenched hands without polydactyly, suggestive of trisomy 13 syndrome. However, the cytogenetic study disclosed 46,XY. The case presented here very well represents pseudotrisomy 13 syndrome and signifies the value of cytogenetic study and genetic counseling.en_US
dc.identifier.citationVejabhuti Choladda, Chuangsuwanich Tuenjai, Sangruchi Tumtip, Limwongse Chanin, Botpibul Suchatree, Kanokpongsakdi Sujin. Pseudotrisomy 13 syndrome : A case report. Siriraj Medical Journal, 2003 Jul; 55(7): 409-413.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/137213
dc.language.isoenen_US
dc.source.urihttps://www.sirirajmedj.com/content_download.php?content_id=1033en_US
dc.subjectPseudotrisomy 13 syndromeen_US
dc.titlePseudotrisomy 13 syndrome : A case report.en_US
dc.typeArticleen_US
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