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病例报告:一只患有遗传性肌强直的混血犬第15外显子存在复杂的变异突变。

Case report: A complex variant mutation in exon 15 in a mixed-breed dog with hereditary myotonia.

作者信息

Eguchi Gabriel Utida, Palumbo Mariana Isa Poci, Cerri Fabrício Moreira, Basso Roberta Martins, de Oliveira-Filho José Paes, Caramalac Silvana Marques, Borges Alexandre Secorun

机构信息

Faculty of Veterinary Medicine and Animal Science, Federal University of Mato Grosso do Sul (UFMS), Campo Grande, MS, Brazil.

Department of Veterinary Clinical Science, School of Veterinary Medicine and Animal Science, São Paulo State University (Unesp), Botucatu, SP, Brazil.

出版信息

Front Vet Sci. 2024 Nov 4;11:1485454. doi: 10.3389/fvets.2024.1485454. eCollection 2024.

Abstract

At 4 months of age, a male dog was presented with a complaint of a stiff gait following a startle response. Neurological examination revealed no deficits, but clinical myotonia was easily induced upon requesting the patient to jump. Additionally, myotonia of the upper lip muscles was observed upon manipulation. Hereditary myotonia was suspected, and electromyography confirmed the presence of myotonic potentials. Genetic testing of the myotonic patient identified a complex of mutations, including c.[1636_1639 delins AACGGG] and c.[1644 A>T], both located in exon 15 of the gene leading to the formation of a premature stop codon. Genetic investigations of the mother and four littermates revealed that, except for one littermate who was wild type, all others carried a copy of the mutated gene. To the best of the authors' knowledge, these mutations have not been previously reported.

摘要

一只4个月大的雄性犬因惊吓反应后步态僵硬前来就诊。神经学检查未发现缺陷,但要求病犬跳跃时很容易诱发临床性肌强直。此外,操作时观察到上唇肌肉存在肌强直。怀疑为遗传性肌强直,肌电图证实存在肌强直电位。对该肌强直病犬进行基因检测,发现了一组突变,包括c.[1636_1639 delins AACGGG]和c.[1644 A>T],两者均位于该基因的第15外显子,导致形成提前终止密码子。对母亲和四只同窝仔犬的基因调查显示,除一只同窝仔犬为野生型外,其他所有犬都携带一份突变基因拷贝。据作者所知,这些突变此前尚未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f996/11571544/305a6450e965/fvets-11-1485454-g0001.jpg

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