Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Caudal duplication syndrome

1 Jan 2013

Abstract excerpt

Caudal duplication syndrome is a rare entity in which structures derived from the embryonic cloaca and notochord are duplicated to various extents. Its prevalence at birth is less than 1 per 100,000. The term caudal duplication encompasses a spectrum of anomalies and is often used to describe incomplete separation of monovular twins or referred to as part of the spectrum of anomalies associated with conjoined...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Spinal Dysraphism and Malformations
Share to Teratomas and Epidermoid Cysts

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 24049755
DOI: 10.4103/2249-4847.116412

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Caudal duplication syndromePMID 24049755Read ↗

Caudal duplication syndrome: a literature review and reappraisal of its pathoembryogenesisSemantic proximity Read ↗

The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.Semantic proximity Read ↗

Embryonic Disruption Syndromes in Dogs: Exploring the Overlap and Divergence of Cantrell Syndrome, Amniotic Bands, and Body Stalk Anomalies.Semantic proximity Read ↗

Fetus with Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of a Novel Association and Review of the Phenotype.Semantic proximity Read ↗

Genetic control of caudal development.Semantic proximity Read ↗

LUMBAR syndrome-OEIS complex overlap: A case series and review.Semantic proximity Read ↗

Prenatal diagnosis of Carpenter syndrome: looking beyond craniosynostosis and polysyndactyly.Semantic proximity Read ↗

Prenatal diagnosis of brainstem anomaliesSemantic proximity Read ↗

Kyphomelic dysplasia, phenotypic variability and presence of a caudal appendage.Semantic proximity Read ↗

Caudal Regression Syndrome—A Review Focusing on Genetic AssociationsSemantic proximity Read ↗

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.Semantic proximity Read ↗

Review of genetic factors in intestinal malrotation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.