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杜氏综合征是一种复杂的疾病,由多种具有不同遗传基础和表型重叠的疾病组成。

Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders.

机构信息

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Rockville, Maryland, United States of America.

Genetic Disease Research Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.

出版信息

PLoS One. 2014 Jun 3;9(6):e98686. doi: 10.1371/journal.pone.0098686. eCollection 2014.

Abstract

Dubowitz syndrome is a rare disorder characterized by multiple congenital anomalies, cognitive delay, growth failure, an immune defect, and an increased risk of blood dyscrasia and malignancy. There is considerable phenotypic variability, suggesting genetic heterogeneity. We clinically characterized and performed exome sequencing and high-density array SNP genotyping on three individuals with Dubowitz syndrome, including a pair of previously-described siblings (Patients 1 and 2, brother and sister) and an unpublished patient (Patient 3). Given the siblings' history of bone marrow abnormalities, we also evaluated telomere length and performed radiosensitivity assays. In the siblings, exome sequencing identified compound heterozygosity for a known rare nonsense substitution in the nuclear ligase gene LIG4 (rs104894419, NM_002312.3:c.2440C>T) that predicts p.Arg814X (MAF:0.0002) and an NM_002312.3:c.613delT variant that predicts a p.Ser205Leufs*29 frameshift. The frameshift mutation has not been reported in 1000 Genomes, ESP, or ClinSeq. These LIG4 mutations were previously reported in the sibling sister; her brother had not been previously tested. Western blotting showed an absence of a ligase IV band in both siblings. In the third patient, array SNP genotyping revealed a de novo ∼ 3.89 Mb interstitial deletion at chromosome 17q24.2 (chr 17:62,068,463-65,963,102, hg18), which spanned the known Carney complex gene PRKAR1A. In all three patients, a median lymphocyte telomere length of ≤ 1st centile was observed and radiosensitivity assays showed increased sensitivity to ionizing radiation. Our work suggests that, in addition to dyskeratosis congenita, LIG4 and 17q24.2 syndromes also feature shortened telomeres; to confirm this, telomere length testing should be considered in both disorders. Taken together, our work and other reports on Dubowitz syndrome, as currently recognized, suggest that it is not a unitary entity but instead a collection of phenotypically similar disorders. As a clinical entity, Dubowitz syndrome will need continual re-evaluation and re-definition as its constituent phenotypes are determined.

摘要

杜氏综合征是一种罕见的疾病,其特征为多种先天性异常、认知障碍、生长发育迟缓、免疫缺陷,以及血液系统紊乱和恶性肿瘤风险增加。该疾病存在相当大的表型变异性,提示其遗传异质性。我们对 3 名杜氏综合征患者进行了临床特征分析,并进行了外显子组测序和高密度 SNP 基因分型,这 3 名患者包括一对已报道的兄弟姐妹(患者 1 和 2,哥哥和妹妹)和一名未发表的患者(患者 3)。鉴于这对兄弟姐妹有骨髓异常病史,我们还评估了端粒长度,并进行了放射敏感性检测。在这对兄弟姐妹中,外显子组测序发现核连接酶基因 LIG4 中已知罕见无义突变的复合杂合性(rs104894419,NM_002312.3:c.2440C>T),该突变预测产生 p.Arg814X(MAF:0.0002)和 NM_002312.3:c.613delT 突变,预测产生 p.Ser205Leufs*29 移码。该移码突变在 1000 Genomes、ESP 或 ClinSeq 中均未报道。这些 LIG4 突变之前在该姐妹患者中被报道过;她的哥哥之前没有接受过检测。Western blot 显示,这对兄弟姐妹的 ligase IV 蛋白均缺失。在第三位患者中,SNP 基因分型显示,17q24.2 染色体上存在新发的约 3.89 Mb 染色体片段缺失(chr17:62,068,463-65,963,102,hg18),该缺失跨越已知的 Carney 综合征基因 PRKAR1A。在所有 3 名患者中,均观察到中位数淋巴细胞端粒长度≤第 1 百分位数,放射敏感性检测显示对电离辐射的敏感性增加。我们的研究表明,除了先天性角化不良症外,LIG4 和 17q24.2 综合征也存在端粒缩短;为了证实这一点,应该考虑在这两种疾病中进行端粒长度检测。总的来说,根据目前对杜氏综合征的认识,我们的研究工作以及其他关于杜氏综合征的报告表明,它不是一个单一的实体,而是一系列表型相似的疾病。作为一个临床实体,杜氏综合征需要不断重新评估和重新定义,因为其组成表型正在确定中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/4043752/8bede1d814d4/pone.0098686.g001.jpg

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