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[Epidermolysis bullosa in a calf].

作者信息

Stocker H, Lott G, Straumann U, Rüsch P

机构信息

Klinik für Geburtshilfe, Jungtier- und Euterkrankheiten, Universität Zürich.

出版信息

Tierarztl Prax. 1995 Apr;23(2):123-6.

PMID:7624852
Abstract

A four-week-old Simmental x Red Holstein calf had lesions of skin and oral mucosa since its first days of life. Where skin or mucosa was exposed to minimal trauma as in oral cavity or over joints, it broke off, forming blisters and erosions. The diagnosis of epidermolysis bullosa, a hereditary disease, was based on clinical and histological findings. Histology pointed to the epidermal form of epidermolysis bullosa, comparable to epidermolysis bullosa simplex in humans.

摘要

相似文献

1
[Epidermolysis bullosa in a calf].
Tierarztl Prax. 1995 Apr;23(2):123-6.
2
Epidermolysis bullosa in animals: a review.动物中的大疱性表皮松解症:综述
Vet Dermatol. 2015 Feb;26(1):3-13, e1-2. doi: 10.1111/vde.12176. Epub 2014 Oct 30.
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Congenital generalized epidermolysis bullosa in a calf.
Zentralbl Veterinarmed A. 1994 Mar;41(2):139-42. doi: 10.1111/j.1439-0442.1994.tb00076.x.
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Epidermolysis bullosa simplex in the Collie dog.柯利犬的单纯性大疱性表皮松解症。
J Am Vet Med Assoc. 1977 Oct 15;171(8):721-7.
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A congenital bovine epidermolysis resembling epidermolysis bullosa simplex of man.
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J Vet Intern Med. 2020 Nov;34(6):2800-2807. doi: 10.1111/jvim.15943. Epub 2020 Nov 2.
7
Dermolytic (dystrophic) epidermolysis bullosa inversa.溶解性(营养不良性)反向大疱性表皮松解症。
Arch Dermatol. 1988 Apr;124(4):544-7.
8
DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattle.兽医学中罕见疾病的DNA诊断:整合素β4基因4.4kb的缺失与夏洛来牛的大疱性表皮松解症相关。
BMC Vet Res. 2015 Mar 4;11:48. doi: 10.1186/s12917-015-0366-0.
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Epidermolysis bullosa acquisita: an autoimmune disease with distinctive immunoultrastructural features.获得性大疱性表皮松解症:一种具有独特免疫超微结构特征的自身免疫性疾病。
Cutis. 1983 Dec;32(6):521-7.
10
Epidermolysis bullosa hereditaria. 5. The ultrastructure of oral mucosa and skin in four cases of the letalis form.
Acta Pathol Microbiol Scand. 1968;74(3):311-24.

引用本文的文献

1
A de novo mutation in KRT5 in a crossbred calf with epidermolysis bullosa simplex.一例具有单纯型大疱性表皮松解症的杂交牛犊中 KRT5 的从头突变。
J Vet Intern Med. 2020 Nov;34(6):2800-2807. doi: 10.1111/jvim.15943. Epub 2020 Nov 2.
2
DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattle.兽医学中罕见疾病的DNA诊断:整合素β4基因4.4kb的缺失与夏洛来牛的大疱性表皮松解症相关。
BMC Vet Res. 2015 Mar 4;11:48. doi: 10.1186/s12917-015-0366-0.
3
Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene.
丹麦赫里福德犊牛的大疱性表皮松解症是由LAMC2基因缺失引起的。
BMC Vet Res. 2015 Feb 7;11:23. doi: 10.1186/s12917-015-0334-8.