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携带聚集蛋白聚糖病相关突变的一家系的外显不全现象。

Variable expressivity in a family with an aggrecanopathy.

机构信息

Shriners Hospitals for Children, Montreal, Quebec, Canada.

出版信息

Mol Genet Genomic Med. 2022 Jan;10(1):e1773. doi: 10.1002/mgg3.1773. Epub 2021 Dec 10.

Abstract

BACKGROUND

Osteochondritis dissecans is a condition wherein there is a subchondral bone lesion that causes pain, inflammation, and cartilage damage. Dominant Familial Osteochondritis Dissecans is a rare and severe form of osteochondritis dissecans (OCD). It is caused by heterozygous pathogenic variants in the gene encoding Aggrecan; ACAN. Aggrecan, a proteoglycan, is an essential component of the articular and growth plate cartilage.

METHODS

Herein, we report three individuals from one family; the proband who presented with short stature, a lower limb bone exostosis, and bilateral knee and elbow OCD at the age of 13 years old. His twin brother presented with isolated short stature and his father with short stature and lumbar disc herniation.

RESULTS

Next-generation sequencing of the ACAN gene in the proband identified a frameshift variant which is also present in the brother and father with short stature. The proband was treated surgically with bilateral elbow microfracture, after the failure of conservative therapy.

CONCLUSION

To the best of our knowledge, this is the first patient with an aggrecanopathy who presents with osteochondritis dissecans due to a frameshift variant. This family presents with variable expressivity which might be attributed to modifier genes.

摘要

背景

剥脱性骨软骨炎是一种存在于软骨下骨病变的病症,可导致疼痛、炎症和软骨损伤。显性家族性剥脱性骨软骨炎是一种罕见且严重的剥脱性骨软骨炎(OCD)形式。它是由编码聚集蛋白聚糖的基因中的杂合致病性变异引起的;ACAN。聚集蛋白聚糖是一种蛋白聚糖,是关节和生长板软骨的重要组成部分。

方法

在此,我们报告了一个家庭中的三个人;先证者在 13 岁时出现身材矮小、下肢骨外生骨疣和双侧膝肘 OCD。他的双胞胎兄弟仅表现为身材矮小,而他的父亲则表现为身材矮小和腰椎间盘突出症。

结果

对先证者的 ACAN 基因进行下一代测序发现了一个移码变异,该变异也存在于身材矮小的兄弟和父亲中。在保守治疗失败后,先证者接受了双侧肘部微骨折手术治疗。

结论

据我们所知,这是第一个因移码变异而出现剥脱性骨软骨炎的聚集蛋白病患者。该家族表现出可变表达性,这可能归因于修饰基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b332/8801139/df1a2e7d407e/MGG3-10-e1773-g007.jpg

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