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首页> 外文期刊>DTW:Deutsche Tierarztliche Wochenschrift >Review on canine elbow dysplasia: pathogenesis, diagnosis, prevalence and genetic aspects.
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Review on canine elbow dysplasia: pathogenesis, diagnosis, prevalence and genetic aspects.

机译:犬肘不典型增生的综述:发病机理,诊断,患病率和遗传因素。

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摘要

Elbow dysplasia (ED) is a progressive skeletal disease, which may comprise osteoarthrotic changes, incongruity of the joint, a fragmented medial coronoid process (FCP), osteochondrosis dissecans of the trochlea humeri (OCD), and an ununited anconeal process (UAP). Disturbances of enchondral ossification, as well as asynchronous growth of the antebrachial bones and an increased growth rate may provoke abnormal stresses on specific locations such as the medial coronoid process, the anconeal process of the ulna or the humeral trochlea, which may result in ED. Overnutrition with calcium, vitamin D and energy had important influence on rapidity of growth and proneness to ED. ED manifests most often in young dogs less than 1 1/2 year, causing clinical signs such as (intermittent) lameness, pain on movement and altered posture of the affected limb, and radiographically secondary osteoarthrotic changes such as osteophytes or the aforementioned primary lesions. As radiographic projection of the primary lesions FCP and OCD may be difficult in the commonly used mediolateral flexed and craniocaudal views, additional projections such as mediolateral extended or anteroposterior oblique views and alternative diagnostic means such as computed tomography (CT) may be worth considering. Cases of ED are reported in various breeds, though some breeds are especially predisposed and seem to be prone to specific primary lesions. For the German shepherd dog, a breed-predisposition for UAP may be explained by broad chondral junction in association with an accelerated pattern of skeletal maturation. Heritabilities were estimated in a variety of studies, depending strongly on the type of model used. The mode of inheritance is not yet ascertained, but recently the common assumption of a polygenic mode of inheritance for ED is doubted. Instead, genetic independence was supposed between different primary lesions, and also for ED as well as for FCP major gene influence was discussed. So long, phenotypic mass selection was accomplished in different countries most often resulting in a reduced prevalence of ED. The use of best linear unbiased prediction (BLUP) methods including information on relatives and separate evaluation of genetically independent primary lesions may further improve selection against ED.
机译:肘关节发育不良(ED)是一种进行性骨骼疾病,可能包括骨关节炎变化,关节不协调,内侧冠状突碎裂(FCP),滑车肱骨剥离性骨软骨病(OCD)和不联合的前突(UAP)。软骨内骨化障碍,前臂骨的异步生长以及生长速率的增加可能会在特定位置引发异常压力,例如内侧冠状突,尺骨的前突或肱骨滑车,可能导致ED。钙,维生素D和能量的营养过剩对生长速度和易发ED有重要影响。 ED最常在不到1 1/2年的幼犬中出现,引起临床症状,如(间歇性)la行,活动疼痛和患肢改变姿势,以及影像学上继发性骨关节炎的变化,例如骨赘或上述原发性病变。由于在通常使用的后外侧屈曲和颅尾镜检查中可能难以对原发病变进行FCP和OCD的放射线照相投影,因此可能值得考虑使用其他投影(例如,中视眼外侧张开或前后斜视)和其他诊断手段,例如计算机断层扫描(CT)。 ED的病例在不同的品种中都有报道,尽管某些品种特别容易患病,并且似乎容易发生特定的原发性病变。对于德国牧羊犬,UAP的品种易感性可以通过宽阔的软骨交界处以及骨骼成熟的加速模式来解释。在各种研究中都估计了遗传力,这在很大程度上取决于所用模型的类型。遗传的方式尚未确定,但是最近人们对ED多基因遗传方式的普遍假设提出了质疑。取而代之的是,假定在不同原发灶之间存在遗传独立性,并讨论了ED以及FCP主要基因的影响。如此长的时间,表型大众化选择是在不同国家完成的,通常导致ED患病率降低。最佳线性无偏预测(BLUP)方法的使用,包括有关亲属的信息以及对遗传独立原发灶的单独评估,可能会进一步改善针对ED的选择。

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