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

IF 2.4 2区 农林科学 Q1 VETERINARY SCIENCES
Ella Baville, Bianca Carstanjen, Aurélie Thomas-Cancian, Anne Calgaro, Nathale Bonnet, Laurent Tiret, Vincent Gache, Marie Abitbol
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引用次数: 0

Abstract

Background: Supernumerary 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.

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

Study design: Retrospective study.

Methods: Forty-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.

Results: On 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.

Conclusions: We 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.

柏柏尔人和阿拉伯-柏柏尔马家族的遗传性非综合征性多指畸形。
背景:在包括人类、野生动物和家畜在内的各种物种中都描述了多余的手指或多指畸形。在马中,它代表了最常见的先天性肢体畸形,这只在孤立的病例或核心家庭中被描述。分子病因尚未见报道。目的:表征非综合征前轴多指畸形在马家族的表型和破译遗传模式。研究设计:回顾性研究。方法:招募43名家庭成员,包括先前报道的多趾病例。总结了最初病例及其家庭成员的临床和放射检查结果,并对马进行了核型检查。结果:在临床检查中,8匹马(包括先前报道的病例)前肢有一或两个多余的手指,另外1例通过x线摄影诊断。所有9匹多趾马的前肢内侧都有额外的指骨。x线摄影突出了单侧或双侧缺陷的可变表达。在多余指骨的数量、基本掌骨的发育水平、多余手指的个体化和基本蹄的存在方面观察到变化。所有9匹受影响的马都与一匹种马有关。家谱分析显示,最可能的遗传模式是常染色体显性,不完全外显和可变表达。不能排除更复杂的模式。主要限制:由于保密限制和亲属的国际分散,限制招募家庭成员,x光片质量。结论:我们描述了柏柏尔人和阿拉伯柏柏尔家族的马前轴多指畸形,最有可能是常染色体显性遗传,不完全外显。这是对马的遗传性非综合征性多指畸形的首次描述。
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来源期刊
Equine Veterinary Journal
Equine Veterinary Journal 农林科学-兽医学
CiteScore
5.10
自引率
13.60%
发文量
161
审稿时长
6-16 weeks
期刊介绍: Equine Veterinary Journal publishes evidence to improve clinical practice or expand scientific knowledge underpinning equine veterinary medicine. This unrivalled international scientific journal is published 6 times per year, containing peer-reviewed articles with original and potentially important findings. Contributions are received from sources worldwide.
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