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一窝美国繁育的英国激飞猎犬中出现的岩藻糖苷贮积症。

Fucosidosis in a family of American-bred English Springer Spaniels.

作者信息

Smith M O, Wenger D A, Hill S L, Matthews J

机构信息

Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins 80523, USA.

出版信息

J Am Vet Med Assoc. 1996 Dec 15;209(12):2088-90.

PMID:8960193
Abstract

Fucosidosis was detected in a family of English Springer Spaniels in the United States. To our knowledge, these are the first reported cases of this disease in American-bred dogs. Affected and carrier status of dogs were determined by measuring the activity of the enzyme alpha-L-fucosidase in plasma and in leukocytes. Fucosidosis results in neurologic signs, particularly changes in behavior, in adolescent and adult dogs. Late onset of signs may result in misdiagnosis as a primary behavior problem or acquired neurologic disease. Fucosidosis is inherited in an autosomal recessive manner, and carrier dogs are clinically normal. Thus, the abnormal gene can become widespread in a population before homozygous-affected dogs are produced.

摘要

在美国的一个英国激飞猎犬家族中检测到了岩藻糖苷贮积症。据我们所知,这些是美国繁育犬中首次报道的该疾病病例。通过测量血浆和白细胞中α-L-岩藻糖苷酶的活性来确定犬的患病和携带状态。岩藻糖苷贮积症会导致青少年和成年犬出现神经症状,尤其是行为改变。症状出现较晚可能会被误诊为原发性行为问题或后天性神经疾病。岩藻糖苷贮积症以常染色体隐性方式遗传,携带该疾病基因的犬在临床上表现正常。因此,在纯合患病犬出现之前,异常基因可能会在种群中广泛传播。

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