Evidence map›Paper›PMID 40629359›Full record

ArticleOrphanet journal of rare diseases2025

Revised orphanet nomenclature and classification for spina bifida and other spinal dysraphisms (SBoD).

Ferdinand Dhombres, Timothée de Saint-Denis, Dominic Thompson, Julie Tahraoui-Bories, Caterina Lucano, Ana Rath, Giovanni Mosiello, Jean-Marie Jouannic, Rennes Workshop #1 attendees, Roma Workshop #2 attendees and 2 more

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Prenatal findings and postnatal outcomes in cases of closed spinal dysraphism: 10-year two-center cohort study.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2026
    Article
  2. Clinical and MR neuroimaging features of lumbosacral spinal malformations: a tertiary care institutional experience in south India.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  3. Article
  4. Evaluating occult spinal dysraphism in children with midline cutaneous lesions: when to image?Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  5. Article
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

12 authors.

Ferdinand Dhombres *Fetal Medicine Department, Armand Trousseau Hospital, APHP Sorbonne University, GRC 26 and INSERM Limics, Paris, France. ferdinand.dhombres@aphp.fr.ORCID http://orcid.org/0000-0003-3246-8727
Timothée de Saint-Denis *Pediatric Neuro-Orthopedic Department, Armand Trousseau Hospital, APHP Sorbonne University, Paris, France.ORCID http://orcid.org/0000-0003-2482-7160
Dominic ThompsonDepartment of Paediatric Neurosurgery, Great Ormond Street Hospital, London, UK.ORCID http://orcid.org/0000-0002-1114-9869
Julie Tahraoui-BoriesINSERM, US14 - Orphanet, Plateforme Maladies Rares, 75014, Paris, France.ORCID http://orcid.org/0000-0001-9725-7141
Caterina LucanoINSERM, US14 - Orphanet, Plateforme Maladies Rares, 75014, Paris, France.ORCID http://orcid.org/0009-0008-3646-7469
Ana RathINSERM, US14 - Orphanet, Plateforme Maladies Rares, 75014, Paris, France.ORCID http://orcid.org/0000-0003-4308-6337
Giovanni MosielloDivision of Neuro-Urology, Bambino Gesù Children's Hospital, IRCCS, 00165, Rome, Italy.ORCID http://orcid.org/0000-0002-9626-9519
Jean-Marie JouannicFetal Medicine Department, Armand Trousseau Hospital, APHP Sorbonne University, GRC 26 and INSERM Limics, Paris, France.ORCID http://orcid.org/0000-0002-7890-3790
Rennes Workshop #1 attendees
Roma Workshop #2 attendees
Barcelona Workshop #3 attendees
ERN network managers

Funding

EU ERN GRANT AGREEMENT 101156380EU ERN GRANT AGREEMENT 101156387
6 · The paper itself

Abstract

backgroundThe Spina Bifida and other Dysraphisms working group (SBoD WG) is an interdisciplinary group, comprising experts on spinal dysraphism from 11 European countries. In 2022, the SBoD WG was tasked by 2 European Rare Disease Networks (ERN ITHACA and ERN eUROGEN) to revise the Orphanet classification of spinal dysraphism. Over the past two decades numerous subcategories of spinal dysraphism have been described in the medical literature resulting in a proliferation of terms, numerous synonyms and variously applied definitions. In the light of this, a revision of all terms and definitions was conducted by a Delphi approach in 3 steps by neurosurgeons (fetal/paediatric/adult), urologists (paediatric/adult), rehabilitation medicine specialists, fetal medicine and perinatal imaging specialists, geneticists, pathologists, nephrologists and patient representatives, all members of the International Federation for Spina Bifida and Hydrocephalus (IFSBH).

resultsIn the first instance, 39 experts reviewed and refined the terminology that could be used to describe the anatomical characteristics of all forms of SBoD. At the second stage, 24 experts established terms and unambiguous definitions for 16 skin findings, 7 bone findings and 33 spinal cord findings that were considered essential features capable of describing all forms of spinal dysraphism. In the third stage, 29 experts validated 24 spinal dysraphic anomalies using these pre-agreed findings. All terms and definitions were validated by vote with a threshold of 80% approval (abstention was permitted). No terms with disagreement were retained in the subsequent classification. The revised SBoD classification was transferred to the Orphanet nomenclature (ORPHA:823). 16 existing ORPHAcodes were deemed obsolete, 10 ORPHAcodes were updated (terms and/or textual definitions) and 25 new ORPHAcodes were created. The SBoD working group also developed a 'decision tree' for new users, to assist them in the practical aspects of applying the revised classification and designating appropriate ORPHAcodes.

conclusionsAn update of the Orphanet Classification of spinal dysraphism was conducted by a European interdisciplinary group of experts encompassing all aspects of healthcare for patients with these disorders. This new classification, based on essential skin, bone and spinal cord findings offers a more logical and reproducible means to categorise SBoD. It is hoped that this will permit more precise disease delineation, consistent diagnostic accuracy and better prognostication.

Indexed as

Spinal DysraphismHumansTerminology as TopicClassificationMyelomeningoceleRare diseaseSpina bifidaSpinal dysraphism

Identifiers

PMID40629359
PMCPMC12239321

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.