Suppr超能文献

通过反向表型分析鉴定的自身免疫性淋巴细胞增生综合征

Autoimmune lymphoproliferative syndrome identified through reverse phenotyping.

作者信息

Kocheva Svetlana, Gjorgijevska Marija, Vujovic Marija, Martinova Kata, Antevska-Trajkova Zorica, Jovanovska Aleksandra, Stavrikj Katarina, Plaseska-Karanfilska Dijana

机构信息

Faculty of Medicine, University Clinic for Children's Diseases, Ss. Cyril and Methodius University in Skopje, North Macedonia.

Research Centre for Genetic Engineering and Biotechnology "Georgi D. Efremov", MASA, Skopje, North Macedonia.

出版信息

Cent Eur J Immunol. 2022;47(2):179-182. doi: 10.5114/ceji.2022.118079. Epub 2022 Jul 15.

Abstract

Autoimmune lymphoproliferative syndrome (ALPS) is a chronic non-malignant lymphoproliferative disorder caused by mutations in the genes involved in programmed cell death. It is inherited as an autosomal dominant pattern with variable penetrance. In this paper we present the first report of a Macedonian family with ALPS, caused by a novel heterozygous variant in the FAS gene. The next generation sequencing (NGS) analysis in a patient with splenomegaly, suspected for hereditary spherocytosis, showed presence of the FAS c.913dupA, p.Thr305AsnfsTer16 variant. The same variant was present in the patient's mother, but not in the mother's parents (proband's grandparents). Thus, the pathogenic FAS variant has arisen as a de novo event in the proband's mother. Later, analysis of the newborn affected sister showed presence of the same FAS variant. Additional clinical and laboratory investigations in the proband and her sister confirmed the presence of specific biomarkers for ALPS. A first-line NGS analysis allows identification of the genetic defect and initiation of appropriate clinical examinations to promptly establish the clinical diagnosis in patients with rare diseases. Reverse phenotyping in our case provided a prompt and accurate diagnosis and early initiation of specific therapy.

摘要

自身免疫性淋巴细胞增生综合征(ALPS)是一种由程序性细胞死亡相关基因突变引起的慢性非恶性淋巴细胞增生性疾病。它以常染色体显性模式遗传,具有可变的外显率。在本文中,我们首次报告了一个患有ALPS的马其顿家族,该家族由FAS基因中的一种新型杂合变异引起。对一名脾肿大、疑似遗传性球形红细胞增多症患者进行的下一代测序(NGS)分析显示存在FAS c.913dupA、p.Thr305AsnfsTer16变异。该患者的母亲也存在相同变异,但患者母亲的父母(先证者的祖父母)中不存在。因此,致病性FAS变异是在先证者母亲中作为新生事件出现的。后来,对受影响的新生儿妹妹进行分析,发现存在相同的FAS变异。对先证者及其妹妹进行的额外临床和实验室检查证实了存在ALPS的特定生物标志物。一线NGS分析能够识别遗传缺陷,并启动适当的临床检查,以便迅速对罕见病患者做出临床诊断。在我们的病例中,反向表型分析提供了快速准确的诊断,并早期启动了特异性治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76dd/9894091/a3bc8a454c92/CEJI-47-47481-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验