A Unique Derivative Chromosome 4 with a Predominant 4p16.3 Microduplication Phenotype and a Literature Review.

IF 0.9 4区 医学 Q4 GENETICS & HEREDITY
Molecular Syndromology Pub Date : 2025-02-01 Epub Date: 2024-08-28 DOI:10.1159/000540454
Mona K Mekkawy, Alaa K Kamel, Khaled M Refaat, Abdelrahman Madian, Mahmoud Issa, Sally G Abd Allah, Ola M Eid, Maha S Zaki, Amal M Mohamed
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引用次数: 0

Abstract

Introduction: Constitutional structural abnormalities affecting chromosome 4 result in variable distinct phenotypic traits including duplication 4p syndrome, deletion 4p or Wolf-Hirschhorn syndrome (WHS), deletion 4q and duplication 4q syndromes. Complex rearrangements involving both chromosome 4 arms are very rarely reported with different break points occurring within regions of 4p13-p16 and 4q32-35. They most commonly occur in familial cases due to parental pericentric inversion resulting in a recombinant chromosome 4 "rec(4)." The clinical picture is dependent on the size and type of copy number imbalance and the genes involved.

Methods: We report on a female patient with delayed developmental milestones and lower limb anomalies, who carried a de novo unique type of complex rearrangement affecting both chromosome 4 arms, diagnosed by karyotype and fluorescence in situ hybridization analysis and chromosomal microarray (CMA).

Results: The chromosome 4 rearrangement involved three copy number alterations, consisting of a terminal 1.17 Mb 4p16.3 deletion with a contiguous proximal 1.8 Mb 4p16.3 duplication, including the Wolf-Hirschhorn critical (WHSC) region, and an inverted 27 Mb terminal 4q32-35.2 duplication attached to terminal 4p. The patient's predominant phenotype was consistent with 4p16.3 microduplication syndrome. The rearrangement occurred as a de novo abnormality, and thus it was designated as a derivative chromosome 4. To the best of our knowledge, this complex type of chromosome 4 rearrangement has not been reported so far.

Conclusion: The present report adds to the scarce 4p16.3 microduplication syndrome reports and emphasizes the role of WHSC region in the syndromic phenotype. It also reveals the importance of CMA in detecting subtle copy number variations (CNVs) that could be dominantly reflected on the phenotype, which is very important in patients' management and family counselling.

具有显性4p16.3微重复表型的独特衍生4号染色体及其文献综述。
简介:影响4号染色体的体质结构异常导致多种不同的表型特征,包括重复4p综合征、缺失4p或沃尔夫-赫希霍恩综合征(WHS)、缺失4q和重复4q综合征。涉及4号染色体两条臂的复杂重排很少报道,不同的断点发生在4p13-p16和4q32-35区域。它们最常发生在家族性病例中,由于亲代中心周围反转导致重组4号染色体(4)。临床表现取决于拷贝数失衡的大小和类型以及所涉及的基因。方法:我们报告了一位患有发育迟缓和下肢异常的女性患者,她携带了一种新的独特类型的复杂重排,影响了4号染色体的两条手臂,通过核型和荧光原位杂交分析和染色体微阵列(CMA)诊断。结果:4号染色体重排涉及3个拷贝数改变,包括末端1.17 Mb的4p16.3缺失和近端1.8 Mb的4p16.3重复,包括Wolf-Hirschhorn临界区,以及末端27 Mb的4q32-35.2重复附着在末端4p上。患者的显性表型符合4p16.3微重复综合征。重排发生为新生异常,因此它被指定为衍生染色体4。据我们所知,这种复杂类型的4号染色体重排到目前为止还没有报道过。结论:本报告补充了稀缺的4p16.3微重复综合征报道,强调了WHSC区域在综合征表型中的作用。这也揭示了CMA在检测细微拷贝数变异(CNVs)方面的重要性,这些变异可能主要反映在表型上,这在患者管理和家庭咨询中非常重要。
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来源期刊
Molecular Syndromology
Molecular Syndromology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
1.70
自引率
9.10%
发文量
67
期刊介绍: ''Molecular Syndromology'' publishes high-quality research articles, short reports and reviews on common and rare genetic syndromes, aiming to increase clinical understanding through molecular insights. Topics of particular interest are the molecular basis of genetic syndromes, genotype-phenotype correlation, natural history, strategies in disease management and novel therapeutic approaches based on molecular findings. Research on model systems is also welcome, especially when it is obviously relevant to human genetics. With high-quality reviews on current topics the journal aims to facilitate translation of research findings to a clinical setting while also stimulating further research on clinically relevant questions. The journal targets not only medical geneticists and basic biomedical researchers, but also clinicians dealing with genetic syndromes. With four Associate Editors from three continents and a broad international Editorial Board the journal welcomes submissions covering the latest research from around the world.
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