Evidence map›Paper›PMID 42089392›Full record

ArticleBirth defects research2026

Sirenomelia: A Review of European Prevalence Data and Epidemiological Analysis of 17 Cases Registered in Wales.

Chris Emmerson, Michael Olson, Ceri Williams, Robert Maddison, David Tucker, Llion Davies, Annie Perraud, Linda Bailey, Ciarán Humphreys, Rhian Hughes and 21 more

Abstract read
In one paragraph

Article in Birth defects research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Chris EmmersonPublic Health Wales, Cardiff, UK.ORCID 0000-0001-6112-7644
Michael OlsonPublic Health Wales, Cardiff, UK.
Ceri WilliamsPublic Health Wales, Cardiff, UK.
Robert MaddisonPublic Health Wales, Cardiff, UK.ORCID 0000-0002-9139-8602
David TuckerPublic Health Wales, Singleton Hospital, Swansea, UK.
Llion DaviesPublic Health Wales, Cardiff, UK.ORCID 0000-0002-4662-7701
Annie PerraudEuropean Commission, Joint Research Centre (JRC), Ispra, Italy.
Linda BaileyPublic Health Wales, Cardiff, UK.
Ciarán HumphreysPublic Health Wales, Carmarthen, UK.
Rhian HughesPublic Health Wales, Carmarthen, UK.
Joanna SichitiuDepartment of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
Madalen Oribe AmoresRegistro Anomalías Congénitas CAV, Subdirección de Salud Pública, Bilbao, Spain.
Ingeborg BarisicChildren's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.
Michele SantoroCNR Institute of Clinical Physiology, Pisa, Italy.
Clara Cavero CarbonellFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO), Centro Superior de Investigación en Salud Pública, Valencia, Spain.
Elizabeth S DraperDepartment of Population Health Sciences, The University of Leicester, Leicester, UK.
Martin HaeuslerStyrian Malformation Registry, Medical University of Graz, Graz, Austria.
Isabelle MonierINSERM U1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), Center of Research in Epidemiology and Statistics, Sorbonne Paris Cité, Paris, France.
Anna Latos-BielenskaDepartment of Medical Genetics, Polish Registry of Congenital Malformations, Poznan, Poland.
Carlos Matias DiasCentro de Estudos e registo de A C, Lisbon, Portugal.
Elly Den HondProvinciaal Instituut voor Hygiene, Antwerp, Belgium.
Elisa BallardiniIMER Registry (Emilia Romagna Registry of Birth Defects), Centre for Clinical and Epidemiological Research, University of Ferrara and Azienda Ospedaliero Univerisitarion di Ferrara, Ferrara, Italy.ORCID 0000-0002-8813-1835
Mary O'MahonyDepartment of Public Health, HSE South (Cork & Kerry), St. Finbarr's Hospital, Cork, Ireland.
Isabelle PerthusCEMC-Auvergne, Chamalieres Cedex, France.
Judith RankinInstitute of Health & Society, Newcastle University, Newcastle upon Tyne, UK.
Anke RissmannMalformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke University, Magdeburg, Germany.
Florence RougetBrittany Registry of Congenital Malformations, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail)-UMR_S 1085, F-35000, Rennes, France.
Sarah StevensNational Congenital Anomaly and Rare Disease Registration Service (NCARDRS), Public Health England, London, UK.
Jorieke E H BergmanDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0002-3929-3619
Diana WellesleyWessex Clinical Genetics Service, Faculty of Medicine, University Hospitals Southampton, Southampton, UK.
Wladimir WerteleckiOMNI-Net for Children, Rivne, Ukraine.ORCID 0000-0001-5864-5985

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSirenomelia is a rare congenital condition most notably characterized by a single lower limb. Previous studies have suggested a prevalence of approximately 1 per 100,000 births. However, in Wales 17 cases were recorded between 1998 and 2016, suggesting a higher rate of sirenomelia in this country.

objectivesThis study compared current prevalence of sirenomelia in Wales with European data. This study further reviewed detailed time, place, and person data on sirenomelia cases in Wales to investigate possible causal factors.

methodA retrospective cohort study from birth defect surveillance programs. Individual-level records for all welsh cases were examined for evidence of causal factors. Comparator data from other countries were obtained from EUROCAT (a European network of population-based registries for the epidemiological surveillance of congenital anomalies).

resultsEuropean data from 24 national and regional registries of congenital anomalies included 97 cases of sirenomelia identified across 9.6 million births between 1998 and 2016, giving a prevalence rate of 1 per 100,000 (95% CI 0.83, 1.23). Five regions reported statistically significantly higher rates than that recorded across all registries, while one region reported a significantly lower rate. Small numbers of cases limit definitive statistical interpretation. Analysis of the Wales data did not identify common epidemiological factors between cases.

conclusionsThe contemporary prevalence of sirenomelia across Europe is consistent with earlier studies at approximately 1 per 100,000 births (95% CI 0.83, 1.23). However, there is greater variation between regions than would be expected by chance. There remains no definitive evidence for causal environmental factors.

Indexed as

EctromeliaEuropeFemaleHumansMalePrevalenceRegistriesRetrospective StudiesWalescongenital abnormalitiesmermaid syndromesirenomeliaWales

Identifiers

PMID42089392
PMCPMC13147492

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