First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant.

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Gabriela Roldão Correia-Costa, Joana Rosa Marques Prota, Antonia Paula Marques-de-Faria, Carlos Eduardo Steiner, Társis Paiva Vieira
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引用次数: 0

Abstract

Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%-5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature. Here, we report a Brazilian male patient with paternal iUPD15 who presented with clinical features consistent with AS and bilateral microphthalmia, the latter attributable to a novel homozygous likely pathogenic variant in ALDH1A3 (NM_000693.4:c.3G>A:p.(Met1?)) unmasked by the isodisomy. Comprehensive molecular investigation, including chromosomal microarray, microsatellite marker analysis, and whole exome sequencing, was essential to elucidate this diagnosis. To the best of our knowledge, this is the first case reported of Angelman syndrome and ALDH1A3-related microphthalmia due to paternal iUPD15. This case highlights the importance of considering UPD in the context of imprinting disorders as well as a mechanism for unveiling recessive diseases.

第15号染色体单系同二体的首次报道揭示天使综合征和小眼症与一种新的纯合ALDH1A3变异相关。
15号染色体父系同位二体(iUPD15)是Angelman综合征(AS)的一个公认原因,约占2%-5%的病例。此外,iUPD的另一个公认的后果是揭示常染色体隐性遗传病。然而,文献中关于iUPD15导致的隐性疾病的报道仍然很少。在这里,我们报告了一名巴西男性患者,父亲患有iUPD15,其临床特征与AS和双侧小眼一致,后者可归因于ALDH1A3的一种新的纯合子可能致病变异(NM_000693.4:c.3G> a:p.(Met1?))被同位异体所揭示。全面的分子研究,包括染色体微阵列、微卫星标记分析和全外显子组测序,对阐明这种诊断至关重要。据我们所知,这是第一例由父亲iUPD15引起的Angelman综合征和aldh1a3相关的小眼症。这个案例强调了在印迹疾病的背景下考虑UPD的重要性,以及揭示隐性疾病的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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