Clarke Lorelei L, Niedringhaus Kevin D, Carmichael K Paige, Keel M Kevin, Fenton Heather
1 Department of Pathology, College of Veterinary Medicine, The University of Georgia, Athens, GA, USA.
2 Southeastern Cooperative Wildlife Disease Study, College of Veterinary Medicine, The University of Georgia, Athens, GA, USA.
Vet Pathol. 2018 Jul;55(4):584-590. doi: 10.1177/0300985818759771. Epub 2018 Feb 14.
Congenital ocular abnormalities in cervids have been previously reported as individual cases from various regions of the United States and include microphthalmia, anophthalmia, congenital cataracts, dermoids, and colobomata. A common underlying cause for these abnormalities, such as nutritional deficiencies, environmental toxin exposures, or genetic mutations, has not been established. This retrospective study summarized and compared cases of suspected congenital ocular abnormalities in free-ranging white-tailed deer ( Odocoileus virginianus) submitted to the Southeastern Cooperative Wildlife Disease Study (SCWDS) in Athens, Georgia, to the preexisting literature. Of 3645 accessions of white-tailed deer submitted to SCWDS, 15 qualifying case records were found. An additional 15 cases were reported previously in the literature. Conditions described in SCWDS cases included microphthalmia (8/15), congenital cataracts (3/15), anophthalmia (2/15), colobomata (1/15), anterior segment dysgenesis (1/15), ectopic lacrimal gland tissue (1/15), and congenital blindness with corneal opacity (1/15). Most (11/15; 73%) of the SCWDS cases were male fawns with an average age of 4 months at presentation, consistent with previously described cases. Most animals had bilateral abnormalities with few extraocular congenital abnormalities, also consistent with existing reports. Cases were variably tested for various infectious agents at the time of submission; 2 cases were seropositive for bluetongue virus. Spatiotemporal clustering of cases was not evident. This study provided a concise and systematic summary of known existing cases of congenital ocular defects in fawns but did not identify a cause.
此前曾有报道称,美国不同地区有个别鹿类出现先天性眼部异常病例,包括小眼症、无眼症、先天性白内障、皮样囊肿和缺损。这些异常的常见潜在原因,如营养缺乏、接触环境毒素或基因突变,尚未明确。这项回顾性研究总结并比较了提交给佐治亚州雅典市东南合作野生动物疾病研究中心(SCWDS)的野生白尾鹿(弗吉尼亚鹿)疑似先天性眼部异常病例,并与现有文献进行了对比。在提交给SCWDS的3645份白尾鹿样本中,发现了15份符合条件的病例记录。文献中此前还报道了另外15例。SCWDS病例中描述的病症包括小眼症(8/15)、先天性白内障(3/15)、无眼症(2/15)、缺损(1/15)、前段发育异常(1/15)、异位泪腺组织(1/15)和伴有角膜混浊的先天性失明(1/15)。大多数(11/15;73%)SCWDS病例为雄性幼鹿,就诊时平均年龄为4个月,这与此前描述的病例一致。大多数动物存在双侧异常,眼外先天性异常较少,这也与现有报道一致。病例提交时对各种感染因子进行了不同程度的检测;2例蓝舌病毒血清检测呈阳性。病例的时空聚集现象不明显。这项研究对已知的幼鹿先天性眼部缺陷现有病例进行了简洁而系统的总结,但未确定病因。