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一种新的、反复出现的、3.6kb 的 PYGL 基因缺失导致糖原贮积症 VI 型。

A Novel, Recurrent, 3.6-kb Deletion in the PYGL Gene Contributes to Glycogen Storage Disease Type VI.

机构信息

Centers for Molecular Medicine, Children's Hospital of Fudan University, Shanghai, China; Institutes of Biomedical Sciences, Children's Hospital of Fudan University, Shanghai, China.

Centers for Molecular Medicine, Children's Hospital of Fudan University, Shanghai, China; Shanghai Key Laboratory of Birth Defects, Pediatrics Research Institute, Children's Hospital of Fudan University, Shanghai, China.

出版信息

J Mol Diagn. 2020 Dec;22(12):1373-1382. doi: 10.1016/j.jmoldx.2020.08.006. Epub 2020 Sep 19.

Abstract

The PYGL gene is the only established gene known to cause glycogen storage disease type VI (GSD6), which is a rare autosomal recessive disorder associated with hepatomegaly, elevated levels of hepatic transaminases, and hypoglycemia. Extended bioinformatics analysis was performed on the exome sequencing data of 5 patients who were clinically diagnosed as having or highly suspected of having GSD, and a single heterozygous pathogenic or likely pathogenic or rare variant of uncertain significance single-nucleotide variant was identified on the PYGL gene. A recurrent, novel, 3.6-kb deletion involving exons 14 to 17 of PYGL was identified in three of the five patients. Together with the two novel and one established stop-gain SNVs, they were diagnosed as compounds heterozygous of PYGL variants and confirmed as GSD6. The detected 3.6-kb deletion was further screened in a Chinese cohort of 31,317 individuals without hepatic abnormalities, and 10 carriers were identified, showing an allele frequency of 0.016%. Compared with the previously established 47 PYGL pathogenic or likely pathogenic SNVs, the novel pathogenic deletion had the second highest allele frequency among the population. This recurrent, novel, 3.6-kb deletion improved the molecular diagnostic rate of the GSD6. The relatively high frequency of the variant suggests that it is a potential mutation hotspot in patients with GSD6.

摘要

PYGL 基因是唯一已知可导致糖原贮积症 VI 型(GSD6)的基因,该病是一种罕见的常染色体隐性遗传疾病,伴有肝肿大、肝转氨酶升高和低血糖。对 5 名临床诊断或高度怀疑患有 GSD 的患者的外显子组测序数据进行了扩展生物信息学分析,在 PYGL 基因上发现了单个杂合致病性或可能致病性或意义不明的罕见变异单核苷酸变异。在这 5 名患者中的 3 名中发现了一种涉及 PYGL 外显子 14 至 17 的反复出现的、新的 3.6kb 缺失。与这两个新的和一个已建立的终止增益 SNV 一起,它们被诊断为 PYGL 变体的复合杂合子,并被确认为 GSD6。在 31,317 名无肝脏异常的中国人群中进一步筛选了该 3.6kb 缺失,发现了 10 名携带者,其等位基因频率为 0.016%。与先前建立的 47 个 PYGL 致病性或可能致病性 SNV 相比,新型致病性缺失在人群中的等位基因频率位居第二。这种反复出现的新型 3.6kb 缺失提高了 GSD6 的分子诊断率。该变体的相对高频提示它可能是 GSD6 患者的潜在突变热点。

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