dnajc21相关的年轻成年女性血小板减少症

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY
Deniz Aslan, Ozlem Akgun-Dogan, Beril Ay, Mahmut Orhun Çamurdan, Hanifenur Mancılar, Yasemin Alanay
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引用次数: 0

摘要

3型骨髓衰竭(BMFS3)(MIM:617052)是由DNAJC21中的纯合致病性变体引起的遗传性骨髓衰竭综合征(IBMFS)的一种亚型。它于2016年首次被定义,迄今为止,已有19名患者被报道。在这里,我们报告了第一位成年患者;一名在DNAJC21中具有新移码变体的20岁女性表现为血小板减少症、畸形表现和卵巢发育不全。我们的患者将临床谱扩展到较轻的一端,并表明DNAJC21相关疾病可能有相对较轻的表现。对儿童和成人持续性非进行性血小板减少症患者的DNAJC21变体的研究将有助于拓宽基因相关表型和基因型谱,并阐明其病理生理学。因此,我们鼓励对未确诊的患者进行随访,以便在成年后提供全外显子组测序(WES)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DNAJC21-related thrombocytopenia in a young adult female

DNAJC21-related thrombocytopenia in a young adult female

Bone marrow failure type 3 (BMFS3) (MIM:617052) is a subtype of inherited bone marrow failure syndromes (IBMFS) caused by homozygous pathogenic variants in DNAJC21. It was first defined in 2016, and to date, 19 patients have been reported. Here we report the first adult patient; a 20-year-old female with a novel frameshift variant in DNAJC21 presents with thrombocytopenia, dysmorphic findings, and ovarian agenesis. Our patient expands the clinical spectrum to the milder end and suggests that DNAJC21-related disorders can have relatively mild presentations. Investigation of DNAJC21 variants in both childhood and adult patients with persistent, non-progressive thrombocytopenia will allow to broaden the gene-related phenotypic and genotypic spectrum and elucidate the pathophysiology. Therefore, we encourage revisiting undiagnosed patients to offer whole exome sequencing (WES) in adulthood.

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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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