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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.

DOI:10.3389/fvets.2024.1485454
PMID:39559538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11571544/
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/b08c91e8975b/fvets-11-1485454-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f996/11571544/305a6450e965/fvets-11-1485454-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f996/11571544/b08c91e8975b/fvets-11-1485454-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f996/11571544/305a6450e965/fvets-11-1485454-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f996/11571544/b08c91e8975b/fvets-11-1485454-g0002.jpg

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本文引用的文献

1
Variants in and Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs.与法国斗牛幼犬肌肉肥大、吞咽困难和步态异常相关的基因变异。
Animals (Basel). 2024 Feb 25;14(5):722. doi: 10.3390/ani14050722.
2
ClC-1 Chloride Channel: Inputs on the Structure-Function Relationship of Myotonia Congenita-Causing Mutations.ClC-1氯离子通道:先天性肌强直致病突变结构-功能关系的研究进展
Biomedicines. 2023 Sep 24;11(10):2622. doi: 10.3390/biomedicines11102622.
3
Hereditary myotonia in cats associated with a new homozygous missense variant p.Ala331Pro in the muscle chloride channel ClC-1.
猫的遗传性肌强直与肌肉氯离子通道 ClC-1 中的新纯合错义变异 p.Ala331Pro 相关。
J Vet Intern Med. 2023 Nov-Dec;37(6):2498-2503. doi: 10.1111/jvim.16837. Epub 2023 Sep 5.
4
A complex variant associated with hereditary myotonia in a mixed-breed dog.与杂种犬遗传性肌强直相关的一种复杂变异。
J Vet Diagn Invest. 2023 Jul;35(4):413-416. doi: 10.1177/10406387231176736. Epub 2023 May 22.
5
A novel mutation of the CLCN1 gene in a cat with myotonia congenita: Diagnosis and treatment.猫先天性肌强直症中 CLCN1 基因突变的新发现:诊断与治疗
J Vet Intern Med. 2022 Jul;36(4):1454-1459. doi: 10.1111/jvim.16471. Epub 2022 Jul 11.
6
Hereditary myotonia in American Bulldog associated with a novel frameshift mutation in the CLCN1 gene.遗传性美国斗牛犬肌强直症与 CLCN1 基因的新型移码突变相关。
Neuromuscul Disord. 2020 Dec;30(12):991-998. doi: 10.1016/j.nmd.2020.10.007. Epub 2020 Oct 24.
7
Paradoxical pseudomyotonia in English Springer and Cocker Spaniels.英国史宾格犬和可卡犬的反常性假肌强直。
J Vet Intern Med. 2020 Jan;34(1):253-257. doi: 10.1111/jvim.15660. Epub 2019 Nov 14.
8
A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigs.一个位于 CLCN1 基因内的大片段缺失导致了猪的遗传性肌强直。
Sci Rep. 2019 Oct 30;9(1):15632. doi: 10.1038/s41598-019-51286-7.
9
Myotonia congenita: mutation spectrum of in Spanish patients.先天性肌强直:西班牙患者的突变谱。
J Genet. 2019 Sep;98.
10
Myotonia congenita in a Labrador Retriever with truncated CLCN1.先天性肌强直症在一只截短型 CLCN1 的拉布拉多猎犬中的表现
Neuromuscul Disord. 2018 Jul;28(7):597-605. doi: 10.1016/j.nmd.2018.05.002. Epub 2018 Jun 19.