Evidence map›Paper›PMID 40348827›Full record

ArticleEuropean journal of human genetics : EJHG2025

Townes-Brocks syndrome: genotype-phenotype correlations of SALL1 variants in our series and the literature.

Fiona Leduc, Perrine Brunelle, Fabienne Escande, Nassima Ramdane, Laurence Bellengier, Léa Giacomello, Christine Lefevre, Aurélie Mezel, Charlotte Samaille, Rony Sfeir and 6 more

Abstract read
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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Townes-Brocks Syndrome as Familial Isolated Bilateral Cup Ear Deformity: A Case Report.Clinical, cosmetic and investigational dermatology · 2026
    Article
  2. Article
  3. Insights in genetics: from molecular mechanisms to patient perspectives.European journal of human genetics : EJHG · 2025
    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

16 authors.

Fiona LeducCHU Lille, University Lille, Clinique de génétique « Guy Fontaine », ULR7364 RADEME, F-59000, Lille, France. fiona.leduc@chu-lille.fr.ORCID 0009-0003-6535-8951
Perrine BrunelleCHU Lille, University Lille, Institut de Génétique médicale, ULR7364 RADEME, F-59000, Lille, France.ORCID 0000-0002-3589-6885
Fabienne EscandeCHU Lille, University Lille, Biochimie et Biologie moléculaire, ULR7364 RADEME, F-59000, Lille, France.
Nassima RamdaneCHU Lille, Department of Biostatistics, F-59000, Lille, France.
Laurence BellengierCHU Lille, University Lille, Clinique de génétique « Guy Fontaine », ULR7364 RADEME, F-59000, Lille, France.
Léa GiacomelloSSR Pédiatrique Marc Sautelet, Médecine Physique et de Réadaptation Fonctionnelle, F-59650, Villeneuve d'Ascq, France.
Christine LefevreCHU Lille, Endocrinologie pédiatrique, Centre de Référence DEV-GEN, F-59000, Lille, France.
Aurélie MezelCHU de Lille, Service de chirurgie orthopédique de l'enfant, F-59000, Lille, France.
Charlotte SamailleCHU Lille, Department of Pediatric Nephrology, Hôpital Jeanne de Flandre, F-59000, Lille, France.
Rony SfeirCHU Lille, University Lille, Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Lille, France, F-59000, Lille, France.
Philippine ToulemondeCHU Lille, University Lille, Department of Otology and Neurotology, Lille, France.ORCID 0000-0001-8774-5424
Rare Disease networks
Sylvie Manouvrier-HanuCHU Lille, University Lille, Clinique de génétique « Guy Fontaine », ULR7364 RADEME, F-59000, Lille, France.
Catherine Vincent-DelormeCHU Lille, University Lille, Clinique de génétique « Guy Fontaine », ULR7364 RADEME, F-59000, Lille, France.
Florence PetitCHU Lille, University Lille, Clinique de génétique « Guy Fontaine », ULR7364 RADEME, F-59000, Lille, France.
Clémence VanlerbergheCHU Lille, University Lille, Clinique de génétique « Guy Fontaine », ULR7364 RADEME, F-59000, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Townes-Brocks syndrome (TBS, MIM#107480) is an autosomal dominant disorder linked to SALL1 alterations and characterized by a clinical triad (anorectal, thumb, and external-ear malformations), along with variable features. Renal failure and deafness can occur at any age, making follow-up essential. Some genotype-phenotype correlations have been suggested but data are limited. We collected clinical and molecular data from 49 patients with a SALL1 (likely) pathogenic variant identified in our laboratory or through collaborations, and reviewed the 207 SALL1 related-TBS patients previously reported in the literature. We performed statistical analysis to study genotype-phenotype correlations based notably on the variant position in relation to the glutamine-rich region. In our series, 25% of individuals presented with the clinical triad compared to 49.7% in the literature. The deafness frequency was similar (65%). Renal failure was diagnosed in 39.6% of our patients compared to 29.3% in the literature. Developmental delay or intellectual disability affected 9% of patients. Of the 22 SALL1 variants in our series, 35% were located upstream of the glutamine-rich region, compared to 6.5% in the literature. Statistical analysis was performed on all patients, of which 26 and 200 carried a variant upstream and downstream of the glutamine-rich region, respectively. A significant increase in deafness, dysplastic ear, and thumb malformations and a significant decrease in renal failure were observed in the individuals carrying a variant located downstream of the region, but the patients were significantly younger. Future studies should aim to elucidate the complex pathophysiological mechanisms and prognosis of TBS, functionally and prospectively.

Indexed as

Abnormalities, MultipleAnus, ImperforateMutationTranscription FactorsAdolescentAdultChildChild, PreschoolFemaleGenetic Association StudiesHearing Loss, SensorineuralHumansInfantMalePhenotypeThumbSALL1 protein, humanTranscription Factors

Identifiers

PMID40348827
PMCPMC12583617

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Registered trials

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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.