Please use this identifier to cite or link to this item: http://adhlui.com.ui.edu.ng/jspui/handle/123456789/4190
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dc.contributor.authorShonubi, AMO-
dc.contributor.authorSalami, BA-
dc.contributor.authorFalade, AG-
dc.contributor.authorEjiwunmi, AB-
dc.date.accessioned2025-05-21T13:48:30Z-
dc.date.available2025-05-21T13:48:30Z-
dc.date.issued2002-
dc.identifier.citationAfr. J. Med. Med. Sci. (2002) 31, 377-379en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/4190-
dc.descriptionArticleen_US
dc.description.abstractA 1,600gm baby with sirenomelia (caudal regression syndrome) associated with extensive anomalies in the internal organs occurring in one of a set of monochromic twins delivered at the Olabisi Onabanjo University Teaching Hospital (OOUTH), Shagamu, Nigeria is being reported. The baby lived for approximately twenty hours. The co-twin had no obvious malformation.en_US
dc.description.sponsorshipCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.language.isoenen_US
dc.publisherCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.subjectSirenomeliaen_US
dc.subjectCaudal regression syndromeen_US
dc.subjectMultiple congenital malformationsen_US
dc.subjectMonochorionic twinsen_US
dc.titleSirenomelia in one of Nigerian monochorionic twinsen_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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