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Complex Body Wall Closure Defects in Seven Dog Fetuses: An Anatomic and CT Scan Study.

dc.contributor.authorMartín Alguacil, María Nieves
dc.contributor.authorCozar, José M
dc.contributor.authorAvedillo Cea, Luis Javier
dc.date.accessioned2025-09-01T15:40:37Z
dc.date.available2025-09-01T15:40:37Z
dc.date.issued2025
dc.descriptionAuthor Contributions: Conceptualization, N.M.-A. and L.A.; methodology, N.M.-A., L.A., and J.M.C.; validation, N.M.-A., L.A., and J.M.C.; formal analysis, N.M.-A., L.A., and J.M.C.; investigation, N.M.- A., L.A., and J.M.C.; data curation, N.M.-A., L.A., and J.M.C.; writing—original draft preparation, N.M.-A.; writing—review and editing, N.M.-A. and L.A.; supervision, N.M.-A. All authors have read and agreed to the published version of the manuscript.
dc.description.abstractBody stalk anomaly (BSA) is a rare and usually fatal congenital disorder involving severe malformations of the body wall, limbs, spine, and internal organs. This study presents the first documented cases of BSA in seven dogs, offering new insights into how the disorder manifests in animals. The affected fetuses consistently exhibited major anomalies, including large abdominal wall defects, structural spinal abnormalities, and a variety of limb malformations ranging from partial agenesis and meromelia to phocomelia and complete amelia. Structural urogenital anomalies and orofacial clefts were also observed, aligning with similar findings in BSA cases reported in pigs and cats. These findings support the hypothesis of a multifactorial etiology involving early embryonic disruptions, such as abnormal folding of the embryo, rupture of the amniotic membrane, and vascular compromise. The frequent occurrence of abdominal wall defects alongside umbilical cord abnormalities further suggests a shared developmental pathway. This study also highlights the value of veterinary cases in comparative embryology and the need to assess congenital anomalies as part of a broader malformation complex. By expanding the phenotypic spectrum of BSA in domestic animals, this work contributes to a deeper understanding of its pathogenesis and emphasizes the importance of further research into the genetic and environmental factors involved. Such efforts could lead to improved classification and diagnosis of complex congenital malformations, as well as facilitate cross-species comparisons.
dc.description.departmentDepto. de Anatomía y Embriología
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationMartín-Alguacil, N., Cozar, J. M., & Avedillo, L. (2025). Complex Body Wall Closure Defects in Seven Dog Fetuses: An Anatomic and CT Scan Study. Animals : an open access journal from MDPI, 15(14), 2030. https://doi.org/10.3390/ani15142030
dc.identifier.doi10.3390/ani15142030
dc.identifier.essn2076-2615
dc.identifier.officialurlhttps://doi.org/10.3390/ani15142030
dc.identifier.pmid40723492
dc.identifier.urihttps://hdl.handle.net/20.500.14352/123582
dc.issue.number2030
dc.journal.titleAnimals
dc.language.isoeng
dc.page.final19
dc.page.initial1
dc.publisherMDPI
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu636.09:611
dc.subject.keywordBSA classification
dc.subject.keywordLBWC
dc.subject.keywordAmniotic bands
dc.subject.keywordBody stalk anomalies (BSAs)
dc.subject.keywordCanine
dc.subject.keywordCraniofacial malformations
dc.subject.keywordNon-structural skeletal anomalies
dc.subject.keywordNon-structural urogenital anomalies
dc.subject.keywordStructural skeletal anomalies
dc.subject.keywordStructural urogenital anomalies
dc.subject.ucmAnatomía veterinaria
dc.subject.unesco2401.01 Anatomía Animal
dc.titleComplex Body Wall Closure Defects in Seven Dog Fetuses: An Anatomic and CT Scan Study.
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number15
dspace.entity.typePublication
relation.isAuthorOfPublicationb19c8f9d-e692-40d3-babb-4da3090b0513
relation.isAuthorOfPublicationdbe46c60-cd10-4fa3-a70e-53512cdcae2d
relation.isAuthorOfPublication.latestForDiscoveryb19c8f9d-e692-40d3-babb-4da3090b0513

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