Dalir-Naghadeh B, Seifi H A, Farshid A A
Department of Clinical Sciences, Faculty of Veterinary Medicine, Urmia University, PO Box 1177, Urmia, Iran.
J Vet Med A Physiol Pathol Clin Med. 2004 Dec;51(9-10):409-12. doi: 10.1111/j.1439-0442.2004.00670.x.
Epitheliogenesis imperfecta is a recessive hereditary condition characterized by the congenital missing of epithelium on the skin and oral mucosa. These lesions vary in size and location but usually consist of irregular patches of discontinuity of hair and squamous epithelium of skin usually on the distal extremities. Affected calves may also have patchy missing epithelium in the oral mucosa and tongue. The defect is usually incompatible with life. In this report, clinical, gross and histopathogical findings of epitheliogenesis imperfecta were described in two neonatal calves and one stillborn calf. Absence of epithelium over extensive areas of limbs, muzzle, nostrils, tongue, hard palate, cheeks and esophagus were among the remarkable findings.
上皮生成不全是一种隐性遗传疾病,其特征是皮肤和口腔黏膜先天性缺乏上皮组织。这些病变的大小和位置各不相同,但通常表现为毛发和皮肤鳞状上皮不连续的不规则斑块,常见于四肢远端。患病犊牛的口腔黏膜和舌头也可能出现片状上皮缺失。这种缺陷通常会导致死亡。在本报告中,描述了两头新生犊牛和一头死产犊牛上皮生成不全的临床、大体和组织病理学表现。四肢、口鼻部、鼻孔、舌头、硬腭、脸颊和食管等大面积区域上皮组织缺失是显著的表现。