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病例报告:吉尔小牛先天性红细胞生成性卟啉病的一个可能病例:临床、病理及分子学研究方法

Case Report: A Possible Case of Congenital Erythropoietic Porphyria in a Gir Calf: A Clinical, Pathological, and Molecular Approach.

作者信息

Queiroz Cintia Regina Rêgo, Machado Mizael, Bromberger Cristiana Raach, Oliveira-Filho Jose Paes, Borges Alexandre Secorun, Soto-Blanco Benito, Borges José Renato Junqueira, Câmara Antônio Carlos Lopes, de Castro Márcio Botelho

机构信息

Veterinary Pathology Laboratory, University of Brasília, Campus Darcy Ribeiro, Brasília, Brazil.

Instituto Nacional de Investigación Agropecuaria, Tacuarembó, Uruguay.

出版信息

Front Vet Sci. 2021 Mar 12;8:632762. doi: 10.3389/fvets.2021.632762. eCollection 2021.

Abstract

Congenital erythropoietic porphyria (CEP) is a rare hereditary autosomal recessive disease which has never been reported in Zebu cattle. A 3-day-old Gir calf showed teeth discoloration, fever, dehydration, and dyspnea. The main gross findings were pink-colored teeth, red-brown periosteum and bone marrow, and a fluorescent bright pink coloration of the bone marrow and articular surfaces under ultraviolet light. Aggregates of periodic acid-Schiff (PAS)-stained porphyrin pigments were evident in the lungs, kidneys, and the liver. An intron 8 single-nucleotide polymorphism (SNP) in both the Gir calf and control animals, along with the absence of the uroporphyrin III synthetase () gene mutation, was observed. Most SNPs were located in the intron regions of the gene without relevance for CEP. A continuous loss of genetic variability and an increase in inbreeding in some herds may be related to CEP in Gir cattle, one of the most prominent Zebu breeds worldwide. In summary, this study describes a presumptive case of CEP in a Gir calf based on clinical and pathological findings. A definitive diagnosis would require the measurement of porphyrin levels in blood, urine, or tissues or the identification of gene defects.

摘要

先天性红细胞生成性卟啉病(CEP)是一种罕见的常染色体隐性遗传性疾病,在瘤牛中从未有过报道。一头3日龄的吉尔小牛出现牙齿变色、发热、脱水和呼吸困难。主要大体检查结果为牙齿呈粉红色、骨膜和骨髓呈红棕色,在紫外线下骨髓和关节表面呈荧光亮粉红色。在肺、肾和肝脏中可见经高碘酸-希夫(PAS)染色的卟啉色素聚集物。在吉尔小牛和对照动物中均观察到第8内含子单核苷酸多态性(SNP),且未发现尿卟啉原III合成酶()基因突变。大多数SNP位于该基因的内含子区域,与CEP无关。一些牛群中遗传变异性的持续丧失和近亲繁殖的增加可能与吉尔牛(全球最著名的瘤牛品种之一)的CEP有关。总之,本研究基于临床和病理检查结果描述了一例吉尔小牛疑似CEP病例。明确诊断需要检测血液、尿液或组织中的卟啉水平或鉴定基因缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d37/7994774/ebea5b49f5d2/fvets-08-632762-g0001.jpg

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