与晚期婴幼儿变性白营养不良症相关的 ARSA 变异及阿什肯纳兹犹太血统个体的携带率。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Rachel Rabin, Yoel Hirsch, Kevin T A Booth, Patricia L Hall, Naomi Yachelevich, Pramod K Mistry, Josef Ekstein, John Pappas
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引用次数: 0

摘要

变色性白质营养不良症(MLD)是一种罕见的神经退行性溶酶体储积病,由 ARSA 基因的双等位致病变体引起。根据发病年龄,MLD 在临床上可分为晚幼型、幼年型和成年型。晚幼年型是最严重的表型,表现为肌张力低下、乏力、步态异常,进而发展为智力和体力衰退,导致早期死亡。MLD被认为是一种泛种族性疾病,以前在阿什肯纳兹犹太人群中没有发现过始祖变体。我们在阿什肯纳兹犹太人后裔中发现了三名同源或复合杂合ARSA基因c.178C>T(p.Arg60Trp)变异体的无关个体,其表型与晚期婴幼儿MLD一致。通过Dor Yeshorim筛查计划计算了93 293名阿什肯纳兹犹太后裔的携带者频率,发现携带者频率为1/1554,即0.06%,这可能是一个创始变异体的代表。分子蛋白质建模显示,该变异影响区域折叠。当ARSA基因中的c.178C>T(p.Arg60Trp)变异出现在同卵或复合杂合状态时,应考虑晚发型MLD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ARSA Variant Associated With Late Infantile Metachromatic Leukodystrophy and Carrier Rate in Individuals of Ashkenazi Jewish Ancestry.

Metachromatic leukodystrophy (MLD) is a rare neurodegenerative lysosomal storage disease resulting from bi-allelic pathogenic variants in the ARSA gene. MLD is distinguished clinically based on the age of onset into late-infantile, juvenile, and adult. The late-infantile type is the most severe phenotype presenting with hypotonia, weakness, gait abnormalities, which progresses to mental and physical decline leading to early death. MLD is considered to be pan-ethnic and no founder variants have previously been described in the Ashkenazi Jewish population. We identified three unrelated individuals of Ashkenazi Jewish descent with homozygosity or compound heterozygosity for the c.178C>T (p.Arg60Trp) variant in the ARSA gene, with a phenotype consistent with late-infantile MLD. The carrier frequency was calculated among 93,293 individuals of Ashkenazi Jewish descent through the Dor Yeshorim screening program and found to have a carrier frequency on 1 in 1554 or 0.06%, which may be representative of a founder variant. Molecular protein modeling showed that the variant affects regional folding. Late-infantile MLD should be considered when the c.178C>T (p.Arg60Trp) variant in the ARSA gene is present in either the homozygous or the compound heterozygous states.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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