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LAMC3 中的复合杂合变异与后部室管膜下结节性异位有关。

Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia.

机构信息

Paediatric and Reproductive Genetics Unit, Women's and Children's Hospital, North Adelaide, SA, Australia.

School of Medicine, University of Adelaide, Adelaide, SA, Australia.

出版信息

BMC Med Genomics. 2021 Feb 27;14(1):64. doi: 10.1186/s12920-021-00911-4.

Abstract

BACKGROUND

Periventricular nodular heterotopia (PNH) is a malformation of cortical development characterized by nodules of abnormally migrated neurons. The cause of posteriorly placed PNH is not well characterised and we present a case that provides insights into the cause of posterior PNH.

CASE PRESENTATION

We report a fetus with extensive posterior PNH in association with biallelic variants in LAMC3. LAMC3 mutations have previously been shown to cause polymicrogyria and pachygyria in the occipital cortex, but not PNH. The occipital location of PNH in our case and the proposed function of LAMC3 in cortical development suggest that the identified LAMC3 variants may be causal of PNH in this fetus.

CONCLUSION

We hypothesise that this finding extends the cortical phenotype associated with LAMC3 and provides valuable insight into genetic cause of posterior PNH.

摘要

背景

室周结节性异位(PNH)是一种皮质发育畸形,其特征为异常迁移神经元的结节。后部 PNH 的病因尚未很好地阐明,我们报告了一例病例,为后部 PNH 的病因提供了一些见解。

病例介绍

我们报告了一例胎儿存在广泛的后部 PNH,伴有 LAMC3 的双等位基因突变。LAMC3 突变先前已被证明可导致枕叶皮质的多微脑回和巨脑回,但不会导致 PNH。我们病例中 PNH 的枕叶位置和 LAMC3 在皮质发育中的拟议功能表明,所鉴定的 LAMC3 变体可能是该胎儿 PNH 的致病原因。

结论

我们假设这一发现扩展了与 LAMC3 相关的皮质表型,并为后部 PNH 的遗传病因提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f516/7916305/cd8dd6abcc7f/12920_2021_911_Fig1_HTML.jpg

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