Evidence map›Paper›PMID 39955445›Full record

ArticleEuropean journal of human genetics : EJHG2025

Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliogenesis.

David Haïm, Nathalie Roux, Lucile Boutaud, Laure Verlin, Chloé Quélin, Candice Moncler, Nicolas Bourgon, Amale Achaiia, Philippe Roth, Pierre Marijon and 3 more

Abstract readCase Reports
In one paragraph

Article in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Spring in EJHG.European journal of human genetics : EJHG · 2025
    Article
  3. Review
  4. Review
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

13 authors.

David HaïmConsultations d'Échographies Prénatales, Centre Hospitalier de Roubaix, Roubaix, France.
Nathalie RouxService de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Lucile BoutaudService de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Laure VerlinINSERM UMR-1163, Institut Imagine, Université Paris Cité, Paris, France.
Chloé QuélinDépartement de Génétique Moléculaire et Génomique, CHU Rennes, Rennes, France.
Candice MonclerINSERM UMR-1163, Institut Imagine, Université Paris Cité, Paris, France.
Nicolas BourgonINSERM UMR-1163, Institut Imagine, Université Paris Cité, Paris, France.
Amale AchaiiaService de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Philippe RothService d'Obstétrique - Maternité, Chirurgie, Médecine et Imagerie Fœtales, Hôpital Necker-Enfants Malades, AP-HP Centre, Paris, France.
Pierre MarijonLaboratoire de Biologie Médicale Multisites SeqOIA, Paris, France.ORCID 0000-0002-6694-6873
Sarah VanlieferinghenHôpital Foch, Suresnes, France.
Sophie ThomasINSERM UMR-1163, Institut Imagine, Université Paris Cité, Paris, France. sophie.thomas@inserm.fr.ORCID 0000-0002-8569-3277
Tania Attié-BitachService de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France. tania.attie@aphp.fr.ORCID 0000-0002-1155-3626

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-IAHU-01Agence Nationale de la Recherche (French National Research Agency) ANR-17-CE16-0003-01Agence Nationale de la Recherche (French National Research Agency) ANR-17-RHUS-0002
6 · The paper itself

Abstract

Ciliopathies are rare genetic diseases marked by considerable phenotypic heterogeneity and overlap. Among the key mechanisms of cilium biology, its compartmentalization is achieved through gating complexes and active transport such as intraflagellar transport (IFT). Among the IFT components, IFT27 plays a role in BBSome-mediated transport of ciliary membrane proteins required for ciliary signaling. While this gene was first linked to Bardet-Biedl syndrome, we next expanded its phenotypic spectrum to a fetal lethal ciliopathy. Here, we identified a second fetal case with short ribs, polydactyly, hypodysplastic kidneys, imperforate anus, and situs inversus. Genome sequencing identified novel biallelic variants in IFT27. Functional analysis of tissues from both fetal cases revealed that all the identified variants lead to mRNA decay. Immunohistochemistry on fetal kidney sections showed that those variants are associated with altered ciliogenesis. Overall, we showed that complete loss of IFT27 function leads to a severe phenotypic spectrum overlapping with short ribs polydactyly and Pallister-Hall syndromes. In addition, our results argue for a role of IFT27 in ciliogenesis in humans.

Indexed as

CiliopathiesPallister-Hall SyndromePhenotypeShort Rib-Polydactyly SyndromeBardet-Biedl SyndromeCiliaHumans

Identifiers

PMID39955445
PMCPMC11894207

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.