两只芬兰拉普亨德幼犬的成骨不全症

IF 1.7 Q2 VETERINARY SCIENCES Veterinary medicine (Auckland, N.Z.) Pub Date : 2021-06-17 eCollection Date: 2021-01-01 DOI:10.2147/VMRR.S308418
Ming Yi Tse, Ian R Porter, Elena Demeter, Erica Behling-Kelly, Joseph J Wakshlag, Andrew D Miller
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摘要

两只 8 周大的芬兰拉普亨德犬在接受治疗时出现疼痛、长骨形态异常、腓骨后突,而且与同窝的狗相比生长发育迟缓。X光片显示多处长骨骨折。临床病理检查显示,该年龄段犬的血清碱性磷酸酶活性异常正常。由于生活质量低下,这些狗被人道安乐死,并进行了全面尸检。解剖发现,所有骨头都很软,很容易折断。组织学检查显示,次生海绵体减小,异常的骨小梁嵌入大量疏松的血管基质中。没有观察到哈弗氏管,骨皮质中含有丰富的编织骨,被纤维血管组织分隔,符合成骨不全症(OI)的诊断。由于母犬和雌犬的后代均为近亲繁殖,因此被怀疑为隐性遗传,该品种的特殊遗传性胶原紊乱症仍有待鉴定。
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Osteogenesis Imperfecta in Two Finnish Lapphund Puppies.

Two 8-week-old Finnish Lapphund dogs presented with pain on manipulation, abnormal long bone conformation, retrognathism, and stunted growth compared to their litter mates. Multiple long bone fractures were evident on radiographs. Clinical pathology showed an atypically normal serum alkaline phosphatase activity for dogs this age. Due to poor quality of life, the dogs were humanely euthanized and subjected to a complete necropsy. On necropsy, all bones were soft and easily broken. Histologic examination revealed that the secondary spongiosa was diminished with abnormal bony trabeculae embedded in abundant loose vascular stroma. No Haversian canals were observed and the cortices contained abundant woven bone separated by fibrovascular tissue consistent with the diagnosis of osteogenesis imperfecta (OI). Inbreeding of the sire and female offspring led to a suspicion of recessive inheritance and the particular genetic collagen disorder remains to be identified in this breed.

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