De Novo Variant in the RPL27 Gene in a Second Infant with Diamond-Blackfan Anemia.

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2024-07-03 eCollection Date: 2024-01-01 DOI:10.1155/2024/6626388
Joshua Glass, Julia Weston, Amy Feldman Lewanda, Suvankar Majumdar
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Abstract

We describe a 10-month-old female with Diamond-Blackfan anemia (DBA) who presented with macrocytic anemia and reticulocytopenia. Whole exome sequencing revealed a de novo intronic variant in RPL27 (NM_000988.3:c.-2-1G > A p.?) previously reported in one individual with DBA. The existing literature suggests the RPL27 gene encodes for a ribosomal protein involved in pre-rRNA processing and erythropoiesis. Further research is needed to assess the functional significance of this variant and its implications for genetic testing and therapeutic strategies. This case expands the clinical spectrum of RPL27-associated DBA and highlights the importance of reclassifying this gene to likely pathogenic.

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第二例菱形黑方贫血症婴儿的 RPL27 基因新变异。
我们描述了一名 10 个月大的女性钻石-贝克范贫血症(DBA)患者,她患有巨幼红细胞性贫血和网织红细胞减少症。全外显子组测序结果显示,RPL27(NM_000988.3:c.-2-1G > A p.?)中存在一个新的内含子变异,该变异曾在一名 DBA 患者中报道过。现有文献表明,RPL27 基因编码一种核糖体蛋白,参与前 RNA 处理和红细胞生成。需要进一步研究评估该变异的功能意义及其对基因检测和治疗策略的影响。该病例扩大了RPL27相关DBA的临床范围,并强调了将该基因重新分类为可能致病基因的重要性。
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发文量
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审稿时长
13 weeks
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