Homozygous variant of MLC1 results in megalencephalic leukoencephalopathy with subcortical cysts

Author:

Zha Jian1ORCID,Chen Yong1,Cao Fangfang1,Xu Yuxin1,Yang Zuozhen2,Wen Shu2,Liang Mengmeng2,Wu Huaping1,Zhong Jianmin1

Affiliation:

1. Department of Neurology Jiangxi Provincial Children's Hospital Nanchang Jiangxi China

2. Cipher Gene LLC Beijing China

Abstract

AbstractBackgroundMegalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare, inherited disorder that causes epilepsy, intellectual disorders, and early onset macrocephaly. MLC1 has been identified as a main pathogenic gene.MethodsClinical data such as magnetic resonance imaging (MRI), routine blood tests, and physical examinations were collected from proband. Trio whole‐exome sequencing (WES) of the family was performed, and all variants with a minor allele frequency (<0.01) in the exon and canonical splicing sites were selected for further pathogenic evaluation. Candidate variants were validated using Sanger sequencing.ResultsHere, we report a new homozygous variant identified in two children from the same family in the MLC1 gene [NM_015166.4: c.838_843delinsATTTTA, (p.Ser280_Phe281delinsIleLeu)]. This variant is classified as variant of uncertain significance (VUS) according to the ACMG guidelines. Further experiments demonstrate that the newly identified variant causes a decrease of MLC1 protein levels when expressed in a heterologous expression system.ConclusionOur case expands on this genetic variation and provides new evidence for the clinical diagnosis of MLC1‐related MLC.

Publisher

Wiley

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