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[瑞士褐牛犊牛的脊髓性肌肉萎缩症]

[Spinal muscular atrophy in Braunvieh calves].

作者信息

Stocker H, Ossent P, Heckmann R, Oertle C

机构信息

Klinik für Geburtshilfe, Jungtier- und Euterkrankheiten mit Ambulatorium, Zürich.

出版信息

Schweiz Arch Tierheilkd. 1992;134(2):97-104.

PMID:1566027
Abstract

Clinical, neurophysiological and histopathological findings of sixteen cases of spinal muscular atrophy in calves are described. The first clinical signs usually were noticed at 2-6 weeks of age. The animals showed weakness in the hindquarters, trembling and ultimate recumbency. There was a marked muscular atrophy in all four extremities. In addition, secondary bronchopneumonia was evident in 11 cases. Histopathological lesions consisted of degenerative changes in the neurons of the ventral horns and the axons of the spinal cord as well as degeneration of nerve axons in the extremities. Neurophysiological measurements revealed spontaneous activity in the muscles of the limbs. The conditions is autosomal recessive. So far 11 bulls have been identified and excluded from breeding.

摘要

描述了16头犊牛脊髓性肌萎缩症病例的临床、神经生理学和组织病理学发现。最初的临床症状通常在2至6周龄时被注意到。动物表现出后躯无力、颤抖并最终卧地不起。所有四肢均有明显的肌肉萎缩。此外,11例出现继发性支气管肺炎。组织病理学病变包括脊髓腹角神经元和轴突的退行性变化以及四肢神经轴突的变性。神经生理学测量显示四肢肌肉有自发活动。该病为常染色体隐性遗传。到目前为止,已鉴定出11头公牛并将其排除在繁殖之外。

相似文献

1
[Spinal muscular atrophy in Braunvieh calves].[瑞士褐牛犊牛的脊髓性肌肉萎缩症]
Schweiz Arch Tierheilkd. 1992;134(2):97-104.
2
[Spinal muscle atrophy in Brown Swiss x Braunvieh cross calves].
Dtsch Tierarztl Wochenschr. 1992 May;99(5):168-75.
3
[A new hereditary disease in Braunvieh cattle in Switzerland: spinal demyelinization (SDM) in calves that remain in lateral recumbency].[瑞士褐牛中的一种新的遗传性疾病:侧卧的犊牛脊髓脱髓鞘(SDM)]
Schweiz Arch Tierheilkd. 1996;138(6):295-300.
4
Spinal muscular atrophy in Brown Swiss calves.
Zentralbl Veterinarmed A. 1989 Dec;36(10):731-8. doi: 10.1111/j.1439-0442.1989.tb00786.x.
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Spinal muscular atrophy in calves of the Red Danish dairy breed.丹麦红牛犊牛的脊髓性肌肉萎缩症
Vet Rec. 1994 Mar 5;134(10):232-5. doi: 10.1136/vr.134.10.232.
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Deletions in the spinal muscular atrophy gene region in a newborn with neuropathy and extreme generalized muscular weakness.一名患有神经病变和极度全身性肌无力的新生儿脊髓性肌萎缩基因区域的缺失。
Eur J Paediatr Neurol. 2000;4(1):35-8. doi: 10.1053/ejpn.1999.0258.
7
Spinal cord degeneration in adult dairy cows associated with the feeding of sorghum beer residues.成年奶牛脊髓退化与高粱啤酒糟喂养有关。
J S Afr Vet Assoc. 1994 Dec;65(4):184-8.
8
Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).运动神经元中Ighmbp2的特征及其对1型呼吸窘迫型人类脊髓性肌萎缩症(SMARD1)小鼠模型发病机制的影响
Hum Mol Genet. 2004 Sep 15;13(18):2031-42. doi: 10.1093/hmg/ddh222. Epub 2004 Jul 21.
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Neuronal vacuolation, myelopathy and laryngeal neuropathy in a mixed-breed dog.一只混种犬出现神经元空泡化、脊髓病和喉神经病变。
J Vet Med A Physiol Pathol Clin Med. 2007 Oct;54(8):445-8. doi: 10.1111/j.1439-0442.2007.00936.x.
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Equine motor neuron disease; a preliminary report.马运动神经元病:初步报告。
Cornell Vet. 1990 Oct;80(4):357-79.

引用本文的文献

1
Spinal Muscular Atrophy in Blonde D'Aquitaine Calves Is Not Associated With FVT1 Gene Mutation.阿基坦 Blonde 犊牛的脊髓性肌肉萎缩与 FVT1 基因突变无关。
Front Vet Sci. 2020 Jun 23;7:348. doi: 10.3389/fvets.2020.00348. eCollection 2020.
2
Mapping of the bovine spinal muscular atrophy locus to Chromosome 24.
Mamm Genome. 2003 Jun;14(6):383-91. doi: 10.1007/s00335-002-3024-3.