Evidence map›Paper›PMID 39853805›Full record

ArticleEquine veterinary journal2025

Inherited non-syndromic polydactyly in a Berber and Arabian-Berber horse family.

Ella Baville, Bianca Carstanjen, Aurélie Thomas-Cancian, Anne Calgaro, Nathale Bonnet, Laurent Tiret, Vincent Gache, Marie Abitbol

Abstract read
In one paragraph

Article in Equine veterinary journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ella BavilleUniversité de Lyon, VetAgro Sup, Marcy l'Etoile, France.
Bianca CarstanjenPferdepraxis, Weilheim, Germany.
Aurélie Thomas-CancianUniversité de Lyon, VetAgro Sup, Marcy l'Etoile, France.
Anne CalgaroUniversité de Toulouse, Genphyse, INRAE, Ecole Nationale Vétérinaire de Toulouse, Toulouse, France.
Nathale BonnetUniversité de Toulouse, Genphyse, INRAE, Ecole Nationale Vétérinaire de Toulouse, Toulouse, France.
Laurent TiretUniversité Paris-Est Créteil, INSERM, EFS, EnvA, IMRB Team Relaix, Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
Vincent GacheUniversité de Lyon, UCBL1 CNRS UMR5261, INSERM U1315, Institut NeuroMyoGene INMG-PNMG Team MNCA, Lyon, France.
Marie AbitbolUniversité de Lyon, VetAgro Sup, Marcy l'Etoile, France.ORCID https://orcid.org/0000-0002-5615-7897

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSupernumerary digits, or polydactyly, have been described in various species including humans, wild and domestic animals. In horses, it represents the most common congenital limb malformation, which has only been described in isolated cases or nuclear families. Molecular aetiology has not been reported.

objectivesTo characterise the phenotype of a non-syndromic pre-axial polydactyly in a horse family and to decipher the inheritance pattern. STUDY

designRetrospective study.

methodsForty-three members of the family including a previously reported polydactyl case were recruited. Available clinical and radiographical findings from the initial case and its family members were summarised and karyotypic examinations of the horses were performed.

resultsOn clinical examination, eight horses (including the previously reported case) had one or two supernumerary digits on their forelimbs and one additional case was diagnosed using radiography. Additional digits were located on the medial side of the forelimbs in all nine polydactyl horses. Radiography highlighted variable expression of the defect, which was either unilateral or bilateral. Variations were observed in the number of supernumerary phalanges, the level of development of a rudimentary metacarpal bone, the individualisation of a supernumerary digit and the existence of a rudimentary hoof. All nine affected horses were related to a single stallion. Pedigree analysis revealed that the most likely inheritance pattern was autosomal dominant with incomplete penetrance and variable expressivity. A more complex mode could not be ruled out. MAIN LIMITATIONS: Restricted recruitment of the family members due to confidentiality constraints and to international dispersal of the relatives, quality of radiographs.

conclusionsWe describe an equine preaxial polydactyly in a Berber and Arabian-Berber family most likely with autosomal dominant inheritance with incomplete penetrance. This is the first description of an inherited non-syndromic polydactyly in horses.

Indexed as

Horse DiseasesPolydactylyAnimalsFemaleForelimbHorsesMalePedigreeRetrospective Studiesdevelopmentdigitgenetichorseinherited diseaselimb

Identifiers

PMID39853805
PMCPMC12508272

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