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产前隐性肌联蛋白病的一系列临床严重程度。

A spectrum of clinical severity of recessive titinopathies in prenatal.

作者信息

Qi Yiming, Ji Xueqi, Ding Hongke, Wang Yunan, Liu Xin, Zhang Yan, Yin Aihua

机构信息

Prenatal Diagnosis Centre, Guangdong Women and Children Hospital, Guangzhou, China.

Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, China.

出版信息

Front Genet. 2023 Jan 25;13:1064474. doi: 10.3389/fgene.2022.1064474. eCollection 2022.

Abstract

Variants in TTN are associated with a broad range of clinical phenotypes, from dominant adult-onset dilated cardiomyopathy to recessive infantile-onset myopathy. However, few foetal cases have been reported for multiple reasons. Next-generation sequencing has facilitated the prenatal identification of a growing number of suspected titinopathy variants. We investigated six affected foetuses from three families, completed the intrauterine course of the serial phenotypic spectrum of TTN, and discussed the genotype-phenotype correlations from a broader perspective. The recognizable prenatal feature onset at the second trimester was started with reduced movement, then contracture 3-6 weeks later, followed with/without hydrops, finally at late pregnancy was accompanied with polyhydramnio (major) or oligohydramnios. Two cases with typical arthrogryposis-hydrops sequences identified a meta-only transcript variant c.36203-1G>T. Deleterious transcriptional consequences of the substitution were verified by minigene splicing analysis. Case 3 identified a homozygous splicing variant in the constitutively expressed Z-disc. It presented a milder phenotype than expected, which was presumably saved by the isoform of corons. A summary of the foetal-onset titinopathy cases implied that variants in TTN present with a series of signs and a spectrum of clinical severity, which followed the dosage/positional effect; the meta-only transcript allele involvement may be a prerequisite for the development of fatal hydrops.

摘要

TTN基因的变异与广泛的临床表型相关,从显性成人起病的扩张型心肌病到隐性婴儿起病的肌病。然而,由于多种原因,胎儿病例报道较少。新一代测序技术有助于产前识别越来越多疑似的肌联蛋白病变异。我们研究了来自三个家庭的六名患病胎儿,完成了TTN基因连续表型谱的宫内病程,并从更广泛的角度讨论了基因型与表型的相关性。可识别的产前特征在孕中期开始,表现为胎动减少,3-6周后出现挛缩,随后伴有或不伴有水肿,妊娠晚期最终伴有羊水过多(主要)或羊水过少。两例典型的关节挛缩-水肿序列病例鉴定出一种仅含meta转录本的变异c.36203-1G>T。通过小基因剪接分析证实了该替代的有害转录后果。病例3在组成性表达的Z盘区鉴定出一个纯合剪接变异。其表现出比预期更轻的表型,这可能是由corons异构体挽救的。胎儿期起病的肌联蛋白病病例总结表明,TTN基因变异表现出一系列体征和临床严重程度谱,遵循剂量/位置效应;仅含meta转录本等位基因的参与可能是致命水肿发生的先决条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f457/9907677/a29d8ef65275/fgene-13-1064474-g001.jpg

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