Síndrome de perfusión arterial retrógrada en gemelos (trap): feto acardio. Reporte de un caso

dc.contributor.authorL F Ávila Ramírez
dc.contributor.authorMaría Luisa Carmona de Uzcátegui
dc.contributor.authorBelkys Chacín
dc.contributor.authorFranklin Moreno
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T17:07:17Z
dc.date.available2026-03-22T17:07:17Z
dc.date.issued2009
dc.description.abstractSUMMARY We presente the case of a 23 year old patient, from Barinas State, II gravida, with a twin monochorial pregnancy, a normal fetus who died for respiratory distress in neonatal period and the other one, was an acardio anceps. The acardius presented absence of heart and lungs, a rudimentary brain, and anomalies of extremities. The dissection showed epidermis with numerous vacuolized cells, edematous dermis and absence of mayor epiploon. The external female genitals were well developed. Radiological screening showed a rudimentary cranium and anomalies of the hands and feet. We reviewed the last 30 years of acardia literature.
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/62293
dc.language.isoes
dc.sourceUniversidad de Los Andes
dc.subjectMedicine
dc.subjectDissection (medical)
dc.subjectFetus
dc.subjectRespiratory distress
dc.subjectAnatomy
dc.subjectSurgery
dc.subjectPregnancy
dc.titleSíndrome de perfusión arterial retrógrada en gemelos (trap): feto acardio. Reporte de un caso
dc.typearticle

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